Linked Data
ClinVar Variation Id:
590249
dbSNP Id:
rs61736890
ExAC:
X:148564661 G / A
gnomAD v2:
X-148564661-G-A
gnomAD v3:
X-149483130-G-A
gnomAD v4:
X-149483130-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.149483130G>A , CM000685.2:g.149483130G>A | GRCh38 |
| NC_000023.10:g.148564661G>A , CM000685.1:g.148564661G>A | GRCh37 |
| NC_000023.9:g.148372566G>A | NCBI36 |
| NG_011900.3:g.27205C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340855.11:c.1269C>T MANE Select | ENSP00000339801.6:p.Pro423= | |
| ENST00000651111.1:c.636C>T | ENSP00000498395.1:p.Pro212= | |
| ENST00000340855.10:c.1269C>T | ENSP00000339801.6:p.Pro423= | |
| ENST00000422081.6:c.636C>T | ENSP00000477056.1:p.Pro212= | |
| ENST00000441880.1:n.376C>T | ||
| NM_000202.6:c.1269C>T | NP_000193.1:p.Pro423= | |
| NM_001166550.2:c.999C>T | NP_001160022.1:p.Pro333= | |
| NM_000202.7:c.1269C>T | NP_000193.1:p.Pro423= | |
| NM_001166550.3:c.999C>T | NP_001160022.1:p.Pro333= | |
| NM_000202.8:c.1269C>T MANE Select | NP_000193.1:p.Pro423= | |
| NM_001166550.4:c.999C>T | NP_001160022.1:p.Pro333= |