HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63832086G>T , CM000679.2:g.63832086G>T | GRCh38 |
NC_000017.10:g.61909446G>T , CM000679.1:g.61909446G>T | GRCh37 |
NC_000017.9:g.59263178G>T | NCBI36 |
NG_053004.1:g.15906C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000448276.7:c.*852C>A MANE Select | ENSP00000392617.2:n.*852C>A | |
ENST00000448276.6:c.*852C>A | ENSP00000392617.2:n.*852C>A | |
ENST00000613943.4:c.2337C>A | ENSP00000483605.1:n.2337C>A | |
NM_001098426.1:c.*852C>A | NP_001091896.1:n.*852C>A | |
XM_005257604.2:c.*852C>A | XP_005257661.2:n.*852C>A | |
NM_001330439.1:c.*852C>A | NP_001317368.1:n.*852C>A | |
NM_001330440.1:c.*852C>A | NP_001317369.1:n.*852C>A | |
NM_001098426.2:c.*852C>A MANE Select | NP_001091896.1:n.*852C>A | |
NM_001330440.2:c.*852C>A | NP_001317369.1:n.*852C>A |