Linked Data
ClinVar Variation Id:
329243
ClinVar RCV Id:
RCV000367432
dbSNP Id:
rs886054435
gnomAD v2:
19-40899721-T-C
gnomAD v3:
19-40393814-T-C
gnomAD v4:
19-40393814-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40393814T>C , CM000681.2:g.40393814T>C | GRCh38 |
| NC_000019.9:g.40899721T>C , CM000681.1:g.40899721T>C | GRCh37 |
| NC_000019.8:g.45591561T>C | NCBI36 |
| NG_007979.1:g.24551A>G , LRG_265:g.24551A>G | |
| NG_051224.1:g.1408A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324001.8:c.*152A>G MANE Select | ENSP00000326018.6:n.*152A>G | |
| ENST00000673881.1:c.*152A>G | ENSP00000501070.1:n.*152A>G | |
| ENST00000674005.2:c.*152A>G | ENSP00000501261.1:n.*152A>G | |
| ENST00000674773.1:c.*152A>G | ENSP00000502579.1:n.*152A>G | |
| ENST00000676076.1:c.4399A>G | ||
| ENST00000676316.1:c.4425A>G | ||
| ENST00000291825.11:c.*4743A>G | ENSP00000291825.6:n.*4743A>G | |
| ENST00000324001.7:c.*152A>G | ENSP00000326018.6:n.*152A>G | |
| NM_020956.2:c.*4743A>G , LRG_265t1:c.*4743A>G | NP_066007.1:n.*4743A>G | |
| NM_181882.2:c.*152A>G , LRG_265t2:c.*152A>G | NP_870998.2:n.*152A>G | |
| XM_011527171.1:c.*152A>G | XP_011525473.1:n.*152A>G | |
| XM_011527171.2:c.*152A>G | XP_011525473.1:n.*152A>G | |
| XM_017027046.1:c.*152A>G | XP_016882535.1:n.*152A>G | |
| XM_017027047.1:c.*152A>G | XP_016882536.1:n.*152A>G | |
| NM_181882.3:c.*152A>G MANE Select | NP_870998.2:n.*152A>G |