Linked Data
ClinVar Variation Id:
343025
ClinVar RCV Id:
RCV000406961
dbSNP Id:
rs117707217
ExAC:
3:124467183 G / T
gnomAD v2:
3-124467183-G-T
gnomAD v3:
3-124748336-G-T
gnomAD v4:
3-124748336-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.124748336G>T , CM000665.2:g.124748336G>T | GRCh38 |
| NC_000003.11:g.124467183G>T , CM000665.1:g.124467183G>T | GRCh37 |
| NC_000003.10:g.125949873G>T | NCBI36 |
| NG_017037.1:g.22971G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000232607.7:c.*4252G>T MANE Select | ENSP00000232607.2:n.*4252G>T | |
| ENST00000232607.6:c.*4252G>T | ENSP00000232607.2:n.*4252G>T | |
| NM_000373.3:c.*4252G>T | NP_000364.1:n.*4252G>T | |
| NR_033434.1:n.5647G>T | ||
| NR_033437.1:n.5900G>T | ||
| XR_001740253.2:n.5929G>T | ||
| NM_000373.4:c.*4252G>T MANE Select | NP_000364.1:n.*4252G>T | |
| NR_033434.2:n.5561G>T | ||
| NR_033437.2:n.5814G>T |