Linked Data
ClinVar Variation Id:
252573
ClinVar RCV Id:
RCV000238744
dbSNP Id:
rs879255368
PubMed:
PMID:28135719
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41984953C>T , CM000681.2:g.41984953C>T | GRCh38 |
| NC_000019.9:g.42489105C>T , CM000681.1:g.42489105C>T | GRCh37 |
| NC_000019.8:g.47180945C>T | NCBI36 |
| NG_008015.1:g.14278G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545399.6:c.997G>A | ENSP00000444688.1:p.Ala333Thr | |
| ENST00000644613.1:c.958G>A | ENSP00000494711.1:p.Ala320Thr | |
| ENST00000648268.1:c.958G>A MANE Select | ENSP00000498113.1:p.Ala320Thr | |
| ENST00000302102.9:c.958G>A | ENSP00000302397.5:p.Ala320Thr | |
| ENST00000441343.5:c.958G>A | ENSP00000411503.1:p.Ala320Thr | |
| ENST00000485672.2:n.271G>A | ||
| ENST00000543770.5:c.991G>A | ENSP00000437577.1:p.Ala331Thr | |
| ENST00000545399.5:c.997G>A | ENSP00000444688.1:p.Ala333Thr | |
| ENST00000602133.5:c.868G>A | ENSP00000471581.1:p.Ala290Thr | |
| NM_001256213.1:c.991G>A | NP_001243142.1:p.Ala331Thr | |
| NM_001256214.1:c.997G>A | NP_001243143.1:p.Ala333Thr | |
| NM_152296.4:c.958G>A | NP_689509.1:p.Ala320Thr | |
| XM_011526991.1:c.868G>A | XP_011525293.1:p.Ala290Thr | |
| NM_152296.5:c.958G>A MANE Select | NP_689509.1:p.Ala320Thr | |
| NM_001256214.2:c.997G>A | NP_001243143.1:p.Ala333Thr | |
| NM_001256213.2:c.991G>A | NP_001243142.1:p.Ala331Thr |