Linked Data
dbSNP Id:
rs189993733
gnomAD v2:
19-41518797-A-G
gnomAD v3:
19-41012892-A-G
gnomAD v4:
19-41012892-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41012892A>G , CM000681.2:g.41012892A>G | GRCh38 |
| NC_000019.9:g.41518797A>G , CM000681.1:g.41518797A>G | GRCh37 |
| NC_000019.8:g.46210637A>G | NCBI36 |
| NG_007929.1:g.26594A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324071.10:c.1294+77A>G MANE Select | ENSP00000324648.2:n.1294+77A>G | |
| ENST00000598834.2:c.1177-81A>G | ||
| ENST00000324071.8:c.1294+77A>G | ENSP00000324648.2:n.1294+77A>G | |
| ENST00000593831.1:c.586+77A>G | ENSP00000470582.1:n.586+77A>G | |
| ENST00000597612.1:n.647+407A>G | ||
| NM_000767.4:c.1294+77A>G | NP_000758.1:n.1294+77A>G | |
| XM_005258569.3:c.1152+407A>G | XP_005258626.1:n.1152+407A>G | |
| XM_006723050.2:c.1294+77A>G | XP_006723113.1:n.1294+77A>G | |
| XM_011526546.1:c.1229A>G | XP_011524848.1:p.Asp410Gly | |
| XM_011526547.1:c.1153-81A>G | XP_011524849.1:n.1153-81A>G | |
| XM_011526548.1:c.814+77A>G | XP_011524850.1:n.814+77A>G | |
| XM_011526549.1:c.703+77A>G | XP_011524851.1:n.703+77A>G | |
| XM_011526550.1:c.694+77A>G | XP_011524852.1:n.694+77A>G | |
| NM_000767.5:c.1294+77A>G MANE Select | NP_000758.1:n.1294+77A>G |