HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442313C>A , CM000666.2:g.177442313C>A | GRCh38 |
NC_000004.11:g.178363467C>A , CM000666.1:g.178363467C>A | GRCh37 |
NC_000004.10:g.178600461C>A | NCBI36 |
NG_011845.2:g.5191G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264595.7:c.63G>T MANE Select | ENSP00000264595.2:p.Val21= | |
ENST00000264595.6:c.63G>T | ENSP00000264595.2:p.Val21= | |
ENST00000506853.5:n.97G>T | ||
ENST00000510955.5:n.97G>T | ||
ENST00000511231.1:n.97G>T | ||
NM_000027.3:c.63G>T | NP_000018.2:p.Val21= | |
NM_001171988.1:c.63G>T | NP_001165459.1:p.Val21= | |
NR_033655.1:n.191G>T | ||
XM_006714123.2:c.63G>T | XP_006714186.1:p.Val21= | |
XR_001741155.2:n.157G>T | ||
NM_000027.4:c.63G>T MANE Select | NP_000018.2:p.Val21= | |
NM_001171988.2:c.63G>T | NP_001165459.1:p.Val21= | |
NR_033655.2:n.125G>T |