dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.14562316C>A , CM000671.2:g.14562316C>A | GRCh38 |
| NC_000009.11:g.14562314C>A , CM000671.1:g.14562314C>A | GRCh37 |
| NC_000009.10:g.14552314C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011517851.1:c.622-6580G>T | XP_011516153.1:n.622-6580G>T | |
| XM_011517852.1:c.622-6580G>T | XP_011516154.1:n.622-6580G>T | |
| XM_011517853.1:c.622-6580G>T | XP_011516155.1:n.622-6580G>T | |
| XM_011517854.1:c.622-6580G>T | XP_011516156.1:n.622-6580G>T | |
| XM_011517855.1:c.622-6580G>T | XP_011516157.1:n.622-6580G>T |