Linked Data
ClinVar Variation Id:
416225
dbSNP Id:
rs372280596
ExAC:
19:40899942 G / A
gnomAD v2:
19-40899942-G-A
gnomAD v3:
19-40394035-G-A
gnomAD v4:
19-40394035-G-A
COSMIC:
COSM1393810
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40394035G>A , CM000681.2:g.40394035G>A | GRCh38 |
| NC_000019.9:g.40899942G>A , CM000681.1:g.40899942G>A | GRCh37 |
| NC_000019.8:g.45591782G>A | NCBI36 |
| NG_007979.1:g.24330C>T , LRG_265:g.24330C>T | |
| NG_051224.1:g.1187C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324001.8:c.4317C>T MANE Select | ENSP00000326018.6:p.Ser1439= | |
| ENST00000673881.1:c.3900C>T | ENSP00000501070.1:p.Ser1300= | |
| ENST00000674005.2:c.4602C>T | ENSP00000501261.1:p.Ser1534= | |
| ENST00000674773.1:c.3900C>T | ENSP00000502579.1:p.Ser1300= | |
| ENST00000675517.1:c.4192C>T | ||
| ENST00000676076.1:c.4178C>T | ||
| ENST00000676260.1:c.4279C>T | ||
| ENST00000676316.1:c.4204C>T | ||
| ENST00000291825.11:c.*4522C>T | ENSP00000291825.6:n.*4522C>T | |
| ENST00000324001.7:c.4317C>T | ENSP00000326018.6:p.Ser1439= | |
| NM_020956.2:c.*4522C>T , LRG_265t1:c.*4522C>T | NP_066007.1:n.*4522C>T | |
| NM_181882.2:c.4317C>T , LRG_265t2:c.4317C>T | NP_870998.2:p.Ser1439= | |
| XM_011527171.1:c.4317C>T | XP_011525473.1:p.Ser1439= | |
| XM_011527171.2:c.4317C>T | XP_011525473.1:p.Ser1439= | |
| XM_017027046.1:c.4215C>T | XP_016882535.1:p.Ser1405= | |
| XM_017027047.1:c.4215C>T | XP_016882536.1:p.Ser1405= | |
| NM_181882.3:c.4317C>T MANE Select | NP_870998.2:p.Ser1439= |