dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.19578424T>A , CM000673.2:g.19578424T>A | GRCh38 |
| NC_000011.9:g.19599971T>A , CM000673.1:g.19599971T>A | GRCh37 |
| NC_000011.8:g.19556547T>A | NCBI36 |
| NG_030347.1:g.232701T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360655.8:c.75+227397T>A | ENSP00000353871.4:n.75+227397T>A | |
| NM_001111018.1:c.75+227397T>A | NP_001104488.1:n.75+227397T>A | |
| XM_011520452.1:c.75+227397T>A | XP_011518754.1:n.75+227397T>A | |
| XM_011520452.2:c.75+227397T>A | XP_011518754.1:n.75+227397T>A | |
| XM_017018520.2:c.75+227397T>A | XP_016874009.1:n.75+227397T>A | |
| XM_017018522.1:c.75+227397T>A | XP_016874011.1:n.75+227397T>A | |
| XM_024448758.1:c.75+227397T>A | XP_024304526.1:n.75+227397T>A | |
| NM_001111018.2:c.75+227397T>A | NP_001104488.1:n.75+227397T>A |