Linked Data
ClinVar Variation Id:
3071199
ClinVar RCV Id:
RCV004014701
dbSNP Id:
rs367971361
gnomAD v2:
19-38976284-G-A
gnomAD v3:
19-38485644-G-A
gnomAD v4:
19-38485644-G-A
COSMIC:
COSM3222371
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38485644G>A , CM000681.2:g.38485644G>A | GRCh38 |
| NC_000019.9:g.38976284G>A , CM000681.1:g.38976284G>A | GRCh37 |
| NC_000019.8:g.43668124G>A | NCBI36 |
| NG_008866.1:g.56945G>A , LRG_766:g.56945G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.4989G>A | ENSP00000471601.2:p.Ser1663= | |
| ENST00000359596.8:c.4989G>A MANE Select | ENSP00000352608.2:p.Ser1663= | |
| ENST00000355481.8:c.4989G>A | ENSP00000347667.3:p.Ser1663= | |
| ENST00000359596.7:c.4989G>A | ENSP00000352608.2:p.Ser1663= | |
| ENST00000360985.7:c.4986G>A | ENSP00000354254.4:p.Ser1662= | |
| NM_000540.2:c.4989G>A , LRG_766t1:c.4989G>A | NP_000531.2:p.Ser1663= | |
| NM_001042723.1:c.4989G>A | NP_001036188.1:p.Ser1663= | |
| XM_006723317.1:c.4989G>A | XP_006723380.1:p.Ser1663= | |
| XM_006723319.1:c.4989G>A | XP_006723382.1:p.Ser1663= | |
| XM_011527204.1:c.4986G>A | XP_011525506.1:p.Ser1662= | |
| XM_011527205.1:c.4989G>A | XP_011525507.1:p.Ser1663= | |
| XM_006723317.2:c.4989G>A | XP_006723380.1:p.Ser1663= | |
| XM_006723319.2:c.4989G>A | XP_006723382.1:p.Ser1663= | |
| XM_011527205.2:c.4989G>A | XP_011525507.1:p.Ser1663= | |
| XR_001753735.1:n.5072G>A | ||
| NM_000540.3:c.4989G>A MANE Select | NP_000531.2:p.Ser1663= | |
| NM_001042723.2:c.4989G>A | NP_001036188.1:p.Ser1663= |