Linked Data
dbSNP Id:
rs1776296506
gnomAD v4:
6-32040930-G-A
MyVariant Identifiers:
chr6:g.32008707G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32040930G>A , CM000668.2:g.32040930G>A | GRCh38 |
| NC_000006.11:g.32008707G>A , CM000668.1:g.32008707G>A | GRCh37 |
| NC_000006.10:g.32116686G>A | NCBI36 |
| NG_007941.2:g.7623G>A | |
| NG_008337.2:g.73445C>T | |
| NG_007941.3:g.7626G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000644719.2:c.1284G>A MANE Select | ENSP00000496625.1:p.Val428= | |
| ENST00000418967.6:c.1284G>A | ENSP00000408860.2:p.Val428= | |
| ENST00000435122.3:c.1194G>A | ENSP00000415043.2:p.Val398= | |
| ENST00000479074.5:n.1425G>A | ||
| ENST00000479730.5:n.1400G>A | ||
| ENST00000483041.5:n.1453G>A | ||
| ENST00000486063.5:n.1263G>A | ||
| NM_000500.7:c.1284G>A | NP_000491.4:p.Val428= | |
| NM_001128590.3:c.1194G>A | NP_001122062.3:p.Val398= | |
| XM_011514314.1:c.879G>A | XP_011512616.1:p.Val293= | |
| NM_000500.9:c.1284G>A MANE Select | NP_000491.4:p.Val428= | |
| NM_001368143.1:c.879G>A | NP_001355072.1:p.Val293= | |
| NM_001368144.1:c.879G>A | NP_001355073.1:p.Val293= | |
| NM_001128590.4:c.1194G>A | NP_001122062.3:p.Val398= | |
| NM_001368143.2:c.879G>A | NP_001355072.1:p.Val293= | |
| NM_001368144.2:c.879G>A | NP_001355073.1:p.Val293= |