HGVS | Genome Assembly |
---|---|
NC_000013.11:g.93260737C>T , CM000675.2:g.93260737C>T | GRCh38 |
NC_000013.10:g.93912990C>T , CM000675.1:g.93912990C>T | GRCh37 |
NC_000013.9:g.92710991C>T | NCBI36 |
NG_011880.1:g.38913C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377047.9:c.160+33121C>T MANE Select | ENSP00000366246.3:n.160+33121C>T | |
ENST00000377047.8:c.160+33121C>T | ENSP00000366246.3:n.160+33121C>T | |
NM_005708.3:c.160+33121C>T | NP_005699.1:n.160+33121C>T | |
NM_005708.4:c.160+33121C>T | NP_005699.1:n.160+33121C>T | |
XM_017020299.2:c.-5271C>T | XP_016875788.1:n.-5271C>T | |
NM_005708.5:c.160+33121C>T MANE Select | NP_005699.1:n.160+33121C>T |