HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442411C>T , CM000666.2:g.177442411C>T | GRCh38 |
NC_000004.11:g.178363565C>T , CM000666.1:g.178363565C>T | GRCh37 |
NC_000004.10:g.178600559C>T | NCBI36 |
NG_011845.2:g.5093G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264595.7:c.-36G>A MANE Select | ENSP00000264595.2:n.-36G>A | |
ENST00000264595.6:c.-36G>A | ENSP00000264595.2:n.-36G>A | |
NM_000027.3:c.-36G>A | NP_000018.2:n.-36G>A | |
NM_001171988.1:c.-36G>A | NP_001165459.1:n.-36G>A | |
NR_033655.1:n.93G>A | ||
XM_006714123.2:c.-36G>A | XP_006714186.1:n.-36G>A | |
XR_001741155.2:n.59G>A | ||
NM_000027.4:c.-36G>A MANE Select | NP_000018.2:n.-36G>A | |
NM_001171988.2:c.-36G>A | NP_001165459.1:n.-36G>A | |
NR_033655.2:n.27G>A |