Linked Data
ClinVar Variation Id:
94329
dbSNP Id:
rs185596534
ExAC:
2:71886111 G / A
gnomAD v2:
2-71886111-G-A
gnomAD v3:
2-71658981-G-A
gnomAD v4:
2-71658981-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71658981G>A , CM000664.2:g.71658981G>A | GRCh38 |
| NC_000002.11:g.71886111G>A , CM000664.1:g.71886111G>A | GRCh37 |
| NC_000002.10:g.71739619G>A | NCBI36 |
| NG_008694.1:g.210359G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.2273G>A | ENSP00000513536.1:p.Arg758His | |
| ENST00000698058.1:c.1490G>A | ENSP00000513537.1:p.Arg497His | |
| ENST00000698059.1:c.1598G>A | ENSP00000513538.1:p.Arg533His | |
| ENST00000258104.8:c.4742G>A MANE Plus Clinical | ENSP00000258104.3:p.Arg1581His | |
| ENST00000410020.8:c.4859G>A MANE Select | ENSP00000386881.3:p.Arg1620His | |
| ENST00000258104.7:c.4742G>A | ENSP00000258104.3:p.Arg1581His | |
| ENST00000394120.6:c.4745G>A | ENSP00000377678.2:p.Arg1582His | |
| ENST00000409366.5:c.4808G>A | ENSP00000386512.1:p.Arg1603His | |
| ENST00000409582.7:c.4856G>A | ENSP00000386547.3:p.Arg1619His | |
| ENST00000409651.5:c.4838G>A | ENSP00000386683.1:p.Arg1613His | |
| ENST00000409744.5:c.4766G>A | ENSP00000386285.1:p.Arg1589His | |
| ENST00000409762.5:c.4793G>A | ENSP00000387137.1:p.Arg1598His | |
| ENST00000410020.7:c.4859G>A | ENSP00000386881.3:p.Arg1620His | |
| ENST00000410041.1:c.4796G>A | ENSP00000386617.1:p.Arg1599His | |
| ENST00000413539.6:c.4835G>A | ENSP00000407046.2:p.Arg1612His | |
| ENST00000429174.6:c.4805G>A | ENSP00000398305.2:p.Arg1602His | |
| ENST00000479049.6:n.1627G>A | ||
| NM_001130455.1:c.4745G>A | NP_001123927.1:p.Arg1582His | |
| NM_001130976.1:c.4700G>A | NP_001124448.1:p.Arg1567His | |
| NM_001130977.1:c.4763G>A | NP_001124449.1:p.Arg1588His | |
| NM_001130978.1:c.4805G>A | NP_001124450.1:p.Arg1602His | |
| NM_001130979.1:c.4835G>A | NP_001124451.1:p.Arg1612His | |
| NM_001130980.1:c.4793G>A | NP_001124452.1:p.Arg1598His | |
| NM_001130981.1:c.4856G>A | NP_001124453.1:p.Arg1619His | |
| NM_001130982.1:c.4838G>A | NP_001124454.1:p.Arg1613His | |
| NM_001130983.1:c.4808G>A | NP_001124455.1:p.Arg1603His | |
| NM_001130984.1:c.4766G>A | NP_001124456.1:p.Arg1589His | |
| NM_001130985.1:c.4796G>A | NP_001124457.1:p.Arg1599His | |
| NM_001130986.1:c.4703G>A | NP_001124458.1:p.Arg1568His | |
| NM_001130987.1:c.4859G>A | NP_001124459.1:p.Arg1620His | |
| NM_003494.3:c.4742G>A | NP_003485.1:p.Arg1581His | |
| XM_005264584.3:c.4901G>A | XP_005264641.1:p.Arg1634His | |
| XM_005264585.3:c.4898G>A | XP_005264642.1:p.Arg1633His | |
| XM_005264584.4:c.4901G>A | XP_005264641.1:p.Arg1634His | |
| XM_005264585.5:c.4898G>A | XP_005264642.1:p.Arg1633His | |
| XR_001738969.1:n.5059G>A | ||
| NM_001130987.2:c.4859G>A MANE Select | NP_001124459.1:p.Arg1620His | |
| NM_001130455.2:c.4745G>A | NP_001123927.1:p.Arg1582His | |
| NM_001130976.2:c.4700G>A | NP_001124448.1:p.Arg1567His | |
| NM_001130977.2:c.4763G>A | NP_001124449.1:p.Arg1588His | |
| NM_001130978.2:c.4805G>A | NP_001124450.1:p.Arg1602His | |
| NM_001130979.2:c.4835G>A | NP_001124451.1:p.Arg1612His | |
| NM_001130980.2:c.4793G>A | NP_001124452.1:p.Arg1598His | |
| NM_001130981.2:c.4856G>A | NP_001124453.1:p.Arg1619His | |
| NM_001130982.2:c.4838G>A | NP_001124454.1:p.Arg1613His | |
| NM_001130983.2:c.4808G>A | NP_001124455.1:p.Arg1603His | |
| NM_001130984.2:c.4766G>A | NP_001124456.1:p.Arg1589His | |
| NM_001130985.2:c.4796G>A | NP_001124457.1:p.Arg1599His | |
| NM_001130986.2:c.4703G>A | NP_001124458.1:p.Arg1568His | |
| NM_003494.4:c.4742G>A MANE Plus Clinical | NP_003485.1:p.Arg1581His |