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