Linked Data
dbSNP Id:
rs775622128
ExAC:
5:13769079 G / C
gnomAD v2:
5-13769079-G-C
gnomAD v4:
5-13768970-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13768970G>C , CM000667.2:g.13768970G>C | GRCh38 |
| NC_000005.9:g.13769079G>C , CM000667.1:g.13769079G>C | GRCh37 |
| NC_000005.8:g.13822079G>C | NCBI36 |
| NG_013081.1:g.180511C>G | |
| NG_013081.2:g.180511C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.9887C>G MANE Select | ENSP00000265104.4:p.Ala3296Gly | |
| ENST00000681290.1:c.9842C>G | ENSP00000505288.1:p.Ala3281Gly | |
| ENST00000265104.4:c.9887C>G | ENSP00000265104.4:p.Ala3296Gly | |
| ENST00000504001.3:n.599C>G | ||
| NM_001369.2:c.9887C>G | NP_001360.1:p.Ala3296Gly | |
| XM_005248262.2:c.9842C>G | XP_005248319.1:p.Ala3281Gly | |
| XM_005248262.3:c.9995C>G | XP_005248319.2:p.Ala3332Gly | |
| XM_017009177.1:c.9995C>G | XP_016864666.1:p.Ala3332Gly | |
| XM_017009178.1:c.8900C>G | XP_016864667.1:p.Ala2967Gly | |
| XM_017009179.2:c.8900C>G | XP_016864668.1:p.Ala2967Gly | |
| XM_017009180.1:c.9995C>G | XP_016864669.1:p.Ala3332Gly | |
| XM_017009181.1:c.9995C>G | XP_016864670.1:p.Ala3332Gly | |
| XM_017009182.1:c.9995C>G | XP_016864671.1:p.Ala3332Gly | |
| XM_017009185.1:c.5084C>G | XP_016864674.1:p.Ala1695Gly | |
| XM_017009186.1:c.4637C>G | XP_016864675.1:p.Ala1546Gly | |
| XM_017009188.1:c.3974C>G | XP_016864677.1:p.Ala1325Gly | |
| XM_024454388.1:c.8900C>G | XP_024310156.1:p.Ala2967Gly | |
| XM_024454389.1:c.8489C>G | XP_024310157.1:p.Ala2830Gly | |
| NM_001369.3:c.9887C>G MANE Select | NP_001360.1:p.Ala3296Gly |