Linked Data
ClinVar Variation Id:
1089897
ClinVar RCV Id:
RCV001408864
dbSNP Id:
rs761332828
ExAC:
5:13770902 G / A
gnomAD v2:
5-13770902-G-A
gnomAD v4:
5-13770793-G-A
COSMIC:
COSM3608969
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13770793G>A , CM000667.2:g.13770793G>A | GRCh38 |
| NC_000005.9:g.13770902G>A , CM000667.1:g.13770902G>A | GRCh37 |
| NC_000005.8:g.13823902G>A | NCBI36 |
| NG_013081.1:g.178688C>T | |
| NG_013081.2:g.178688C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.9561C>T MANE Select | ENSP00000265104.4:p.Phe3187= | |
| ENST00000681290.1:c.9516C>T | ENSP00000505288.1:p.Phe3172= | |
| ENST00000265104.4:c.9561C>T | ENSP00000265104.4:p.Phe3187= | |
| ENST00000504001.3:n.273C>T | ||
| NM_001369.2:c.9561C>T | NP_001360.1:p.Phe3187= | |
| XM_005248262.2:c.9516C>T | XP_005248319.1:p.Phe3172= | |
| XM_005248262.3:c.9669C>T | XP_005248319.2:p.Phe3223= | |
| XM_017009177.1:c.9669C>T | XP_016864666.1:p.Phe3223= | |
| XM_017009178.1:c.8574C>T | XP_016864667.1:p.Phe2858= | |
| XM_017009179.2:c.8574C>T | XP_016864668.1:p.Phe2858= | |
| XM_017009180.1:c.9669C>T | XP_016864669.1:p.Phe3223= | |
| XM_017009181.1:c.9669C>T | XP_016864670.1:p.Phe3223= | |
| XM_017009182.1:c.9669C>T | XP_016864671.1:p.Phe3223= | |
| XM_017009183.1:c.9669C>T | XP_016864672.1:p.Phe3223= | |
| XM_017009185.1:c.4758C>T | XP_016864674.1:p.Phe1586= | |
| XM_017009186.1:c.4311C>T | XP_016864675.1:p.Phe1437= | |
| XM_017009188.1:c.3648C>T | XP_016864677.1:p.Phe1216= | |
| XM_024454388.1:c.8574C>T | XP_024310156.1:p.Phe2858= | |
| XM_024454389.1:c.8163C>T | XP_024310157.1:p.Phe2721= | |
| NM_001369.3:c.9561C>T MANE Select | NP_001360.1:p.Phe3187= |