Linked Data
ClinVar Variation Id:
336974
dbSNP Id:
rs763309812
ExAC:
2:71887710 C / T
gnomAD v2:
2-71887710-C-T
gnomAD v3:
2-71660580-C-T
gnomAD v4:
2-71660580-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71660580C>T , CM000664.2:g.71660580C>T | GRCh38 |
| NC_000002.11:g.71887710C>T , CM000664.1:g.71887710C>T | GRCh37 |
| NC_000002.10:g.71741218C>T | NCBI36 |
| NG_008694.1:g.211958C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.2346C>T | ENSP00000513536.1:p.Ile782= | |
| ENST00000698058.1:c.1563C>T | ENSP00000513537.1:p.Ile521= | |
| ENST00000698059.1:c.1671C>T | ENSP00000513538.1:p.Ile557= | |
| ENST00000258104.8:c.4815C>T MANE Plus Clinical | ENSP00000258104.3:p.Ile1605= | |
| ENST00000410020.8:c.4932C>T MANE Select | ENSP00000386881.3:p.Ile1644= | |
| ENST00000258104.7:c.4815C>T | ENSP00000258104.3:p.Ile1605= | |
| ENST00000394120.6:c.4818C>T | ENSP00000377678.2:p.Ile1606= | |
| ENST00000409366.5:c.4881C>T | ENSP00000386512.1:p.Ile1627= | |
| ENST00000409582.7:c.4929C>T | ENSP00000386547.3:p.Ile1643= | |
| ENST00000409651.5:c.4911C>T | ENSP00000386683.1:p.Ile1637= | |
| ENST00000409744.5:c.4839C>T | ENSP00000386285.1:p.Ile1613= | |
| ENST00000409762.5:c.4866C>T | ENSP00000387137.1:p.Ile1622= | |
| ENST00000410020.7:c.4932C>T | ENSP00000386881.3:p.Ile1644= | |
| ENST00000410041.1:c.4869C>T | ENSP00000386617.1:p.Ile1623= | |
| ENST00000413539.6:c.4908C>T | ENSP00000407046.2:p.Ile1636= | |
| ENST00000429174.6:c.4878C>T | ENSP00000398305.2:p.Ile1626= | |
| ENST00000479049.6:n.1700C>T | ||
| NM_001130455.1:c.4818C>T | NP_001123927.1:p.Ile1606= | |
| NM_001130976.1:c.4773C>T | NP_001124448.1:p.Ile1591= | |
| NM_001130977.1:c.4836C>T | NP_001124449.1:p.Ile1612= | |
| NM_001130978.1:c.4878C>T | NP_001124450.1:p.Ile1626= | |
| NM_001130979.1:c.4908C>T | NP_001124451.1:p.Ile1636= | |
| NM_001130980.1:c.4866C>T | NP_001124452.1:p.Ile1622= | |
| NM_001130981.1:c.4929C>T | NP_001124453.1:p.Ile1643= | |
| NM_001130982.1:c.4911C>T | NP_001124454.1:p.Ile1637= | |
| NM_001130983.1:c.4881C>T | NP_001124455.1:p.Ile1627= | |
| NM_001130984.1:c.4839C>T | NP_001124456.1:p.Ile1613= | |
| NM_001130985.1:c.4869C>T | NP_001124457.1:p.Ile1623= | |
| NM_001130986.1:c.4776C>T | NP_001124458.1:p.Ile1592= | |
| NM_001130987.1:c.4932C>T | NP_001124459.1:p.Ile1644= | |
| NM_003494.3:c.4815C>T | NP_003485.1:p.Ile1605= | |
| XM_005264584.3:c.4974C>T | XP_005264641.1:p.Ile1658= | |
| XM_005264585.3:c.4971C>T | XP_005264642.1:p.Ile1657= | |
| XM_005264584.4:c.4974C>T | XP_005264641.1:p.Ile1658= | |
| XM_005264585.5:c.4971C>T | XP_005264642.1:p.Ile1657= | |
| XR_001738969.1:n.5132C>T | ||
| NM_001130987.2:c.4932C>T MANE Select | NP_001124459.1:p.Ile1644= | |
| NM_001130455.2:c.4818C>T | NP_001123927.1:p.Ile1606= | |
| NM_001130976.2:c.4773C>T | NP_001124448.1:p.Ile1591= | |
| NM_001130977.2:c.4836C>T | NP_001124449.1:p.Ile1612= | |
| NM_001130978.2:c.4878C>T | NP_001124450.1:p.Ile1626= | |
| NM_001130979.2:c.4908C>T | NP_001124451.1:p.Ile1636= | |
| NM_001130980.2:c.4866C>T | NP_001124452.1:p.Ile1622= | |
| NM_001130981.2:c.4929C>T | NP_001124453.1:p.Ile1643= | |
| NM_001130982.2:c.4911C>T | NP_001124454.1:p.Ile1637= | |
| NM_001130983.2:c.4881C>T | NP_001124455.1:p.Ile1627= | |
| NM_001130984.2:c.4839C>T | NP_001124456.1:p.Ile1613= | |
| NM_001130985.2:c.4869C>T | NP_001124457.1:p.Ile1623= | |
| NM_001130986.2:c.4776C>T | NP_001124458.1:p.Ile1592= | |
| NM_003494.4:c.4815C>T MANE Plus Clinical | NP_003485.1:p.Ile1605= |