Linked Data
dbSNP Id:
rs1278346713
gnomAD v2:
6-105443901-A-G
gnomAD v3:
6-104996026-A-G
gnomAD v4:
6-104996026-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.104996026A>G , CM000668.2:g.104996026A>G | GRCh38 |
| NC_000006.11:g.105443901A>G , CM000668.1:g.105443901A>G | GRCh37 |
| NC_000006.10:g.105550594A>G | NCBI36 |
| NG_032815.1:g.43979A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345080.5:c.199-30272A>G MANE Select | ENSP00000344401.4:n.199-30272A>G | |
| ENST00000635857.1:c.256-30272A>G | ENSP00000489735.1:n.256-30272A>G | |
| ENST00000637759.1:c.223-30272A>G | ENSP00000490468.1:n.223-30272A>G | |
| ENST00000345080.4:c.199-30272A>G | ENSP00000344401.4:n.199-30272A>G | |
| NM_001004317.3:c.199-30272A>G | NP_001004317.1:n.199-30272A>G | |
| XM_006715477.2:c.256-30272A>G | XP_006715540.2:n.256-30272A>G | |
| XM_011535818.1:c.223-30272A>G | XP_011534120.1:n.223-30272A>G | |
| XM_011535818.3:c.223-30272A>G | XP_011534120.1:n.223-30272A>G | |
| NM_001004317.4:c.199-30272A>G MANE Select | NP_001004317.1:n.199-30272A>G |