HGVS | Genome Assembly |
---|---|
NC_000020.11:g.63895240G>C , CM000682.2:g.63895240G>C | GRCh38 |
NC_000020.10:g.62526593G>C , CM000682.1:g.62526593G>C | GRCh37 |
NC_000020.9:g.61997037G>C | NCBI36 |
NG_029805.1:g.5139G>C | |
NG_029805.2:g.5139G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360864.9:c.-95G>C MANE Select | ENSP00000354111.4:n.-95G>C | |
ENST00000360864.8:c.-95G>C | ENSP00000354111.4:n.-95G>C | |
ENST00000470551.1:c.-95G>C | ENSP00000434744.1:n.-95G>C | |
NM_025219.2:c.-95G>C | NP_079495.1:n.-95G>C | |
NM_025219.3:c.-95G>C MANE Select | NP_079495.1:n.-95G>C |