HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15440531T>C , CM000663.2:g.15440531T>C | GRCh38 |
NC_000001.10:g.15767027T>C , CM000663.1:g.15767027T>C | GRCh37 |
NC_000001.9:g.15639614T>C | NCBI36 |
NG_009253.1:g.7090T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375949.5:c.171T>C MANE Select | ENSP00000365116.4:p.His57= | |
ENST00000375943.6:c.41-1916T>C | ENSP00000365110.2:n.41-1916T>C | |
ENST00000375949.4:c.171T>C | ENSP00000365116.4:p.His57= | |
ENST00000476813.5:n.53-1916T>C | ||
ENST00000483406.1:n.81T>C | ||
NM_007272.2:c.171T>C | NP_009203.2:p.His57= | |
XM_011540550.1:c.171T>C | XP_011538852.1:p.His57= | |
NM_007272.3:c.171T>C MANE Select | NP_009203.2:p.His57= |