Linked Data
dbSNP Id:
rs1295571414
gnomAD v2:
3-183777925-G-A
gnomAD v3:
3-184060137-G-A
gnomAD v4:
3-184060137-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184060137G>A , CM000665.2:g.184060137G>A | GRCh38 |
| NC_000003.11:g.183777925G>A , CM000665.1:g.183777925G>A | GRCh37 |
| NC_000003.10:g.185260619G>A | NCBI36 |
| NG_012749.1:g.12091G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000318351.2:c.1142-13G>A MANE Select | ENSP00000322617.1:n.1142-13G>A | |
| ENST00000318351.1:c.1142-13G>A | ENSP00000322617.1:n.1142-13G>A | |
| NM_130770.2:c.1142-13G>A | NP_570126.2:n.1142-13G>A | |
| NM_130770.3:c.1142-13G>A MANE Select | NP_570126.2:n.1142-13G>A |