Linked Data
dbSNP Id:
rs2241368
gnomAD v2:
5-167835390-A-G
gnomAD v3:
5-168408385-A-G
gnomAD v4:
5-168408385-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.168408385A>G , CM000667.2:g.168408385A>G | GRCh38 |
| NC_000005.9:g.167835390A>G , CM000667.1:g.167835390A>G | GRCh37 |
| NC_000005.8:g.167767968A>G | NCBI36 |
| NG_016712.1:g.121326A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000265293.9:c.721-122A>G MANE Select | ENSP00000265293.4:n.721-122A>G | |
| ENST00000265293.8:c.721-122A>G | ENSP00000265293.4:n.721-122A>G | |
| ENST00000393895.7:c.605-122A>G | ||
| ENST00000517425.5:n.56-122A>G | ||
| ENST00000519659.5:n.71-122A>G | ||
| ENST00000521089.5:c.721-122A>G | ENSP00000427772.1:n.721-122A>G | |
| ENST00000523043.5:n.498-122A>G | ||
| ENST00000524228.5:c.50-122A>G | ||
| NM_001161661.1:c.721-122A>G | NP_001155133.1:n.721-122A>G | |
| NM_001161662.1:c.721-122A>G | NP_001155134.1:n.721-122A>G | |
| NM_015238.2:c.721-122A>G | NP_056053.1:n.721-122A>G | |
| XM_005265850.1:c.721-122A>G | XP_005265907.1:n.721-122A>G | |
| XM_005265853.1:c.721-122A>G | XP_005265910.1:n.721-122A>G | |
| XM_011534485.1:c.721-122A>G | XP_011532787.1:n.721-122A>G | |
| XM_011534486.1:c.721-122A>G | XP_011532788.1:n.721-122A>G | |
| XM_011534487.1:c.721-122A>G | XP_011532789.1:n.721-122A>G | |
| XM_011534488.1:c.721-122A>G | XP_011532790.1:n.721-122A>G | |
| XM_011534489.1:c.721-122A>G | XP_011532791.1:n.721-122A>G | |
| XM_011534490.1:c.721-122A>G | XP_011532792.1:n.721-122A>G | |
| XM_011534491.1:c.721-122A>G | XP_011532793.1:n.721-122A>G | |
| XM_005265853.2:c.721-122A>G | XP_005265910.1:n.721-122A>G | |
| XM_017009276.1:c.721-122A>G | XP_016864765.1:n.721-122A>G | |
| XM_017009278.1:c.439-122A>G | XP_016864767.1:n.439-122A>G | |
| NM_001161661.2:c.721-122A>G | NP_001155133.1:n.721-122A>G | |
| NM_001161662.2:c.721-122A>G | NP_001155134.1:n.721-122A>G | |
| NM_015238.3:c.721-122A>G MANE Select | NP_056053.1:n.721-122A>G |