Linked Data
dbSNP Id:
rs1333102292
gnomAD v2:
2-31754356-C-T
gnomAD v3:
2-31529286-C-T
gnomAD v4:
2-31529286-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31529286C>T , CM000664.2:g.31529286C>T | GRCh38 |
| NC_000002.11:g.31754356C>T , CM000664.1:g.31754356C>T | GRCh37 |
| NC_000002.10:g.31607860C>T | NCBI36 |
| NG_008365.1:g.56686G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000622030.2:c.698+21G>A MANE Select | ENSP00000477587.1:n.698+21G>A | |
| ENST00000622030.1:c.698+21G>A | ENSP00000477587.1:n.698+21G>A | |
| NM_000348.3:c.698+21G>A | NP_000339.2:n.698+21G>A | |
| XM_011533069.1:c.476+21G>A | XP_011531371.1:n.476+21G>A | |
| XM_011533070.1:c.443+21G>A | XP_011531372.1:n.443+21G>A | |
| XM_011533071.1:c.443+21G>A | XP_011531373.1:n.443+21G>A | |
| XM_011533072.1:c.443+21G>A | XP_011531374.1:n.443+21G>A | |
| XM_011533069.2:c.476+21G>A | XP_011531371.1:n.476+21G>A | |
| XM_011533072.2:c.443+21G>A | XP_011531374.1:n.443+21G>A | |
| NM_000348.4:c.698+21G>A MANE Select | NP_000339.2:n.698+21G>A |