Linked Data
ClinVar Variation Id:
2140647
ClinVar RCV Id:
RCV003056553
dbSNP Id:
rs782371096
ExAC:
X:148564596 C / T
gnomAD v2:
X-148564596-C-T
gnomAD v3:
X-149483065-C-T
gnomAD v4:
X-149483065-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.149483065C>T , CM000685.2:g.149483065C>T | GRCh38 |
| NC_000023.10:g.148564596C>T , CM000685.1:g.148564596C>T | GRCh37 |
| NC_000023.9:g.148372501C>T | NCBI36 |
| NG_011900.3:g.27270G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340855.11:c.1334G>A MANE Select | ENSP00000339801.6:p.Arg445His | |
| ENST00000651111.1:c.701G>A | ENSP00000498395.1:p.Arg234His | |
| ENST00000340855.10:c.1334G>A | ENSP00000339801.6:p.Arg445His | |
| ENST00000422081.6:c.701G>A | ENSP00000477056.1:p.Arg234His | |
| NM_000202.6:c.1334G>A | NP_000193.1:p.Arg445His | |
| NM_001166550.2:c.1064G>A | NP_001160022.1:p.Arg355His | |
| NM_000202.7:c.1334G>A | NP_000193.1:p.Arg445His | |
| NM_001166550.3:c.1064G>A | NP_001160022.1:p.Arg355His | |
| NM_000202.8:c.1334G>A MANE Select | NP_000193.1:p.Arg445His | |
| NM_001166550.4:c.1064G>A | NP_001160022.1:p.Arg355His |