HGVS | Genome Assembly |
---|---|
NC_000007.14:g.100647263C>A , CM000669.2:g.100647263C>A | GRCh38 |
NC_000007.13:g.100244886C>A , CM000669.1:g.100244886C>A | GRCh37 |
NC_000007.12:g.100082822C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000160382.10:c.781G>T MANE Select | ENSP00000160382.5:p.Ala261Ser | |
ENST00000160382.9:c.781G>T | ENSP00000160382.5:p.Ala261Ser | |
ENST00000487125.1:n.317G>T | ||
NM_016188.4:c.781G>T | NP_057272.1:p.Ala261Ser | |
XR_927476.1:n.888G>T | ||
NR_134539.1:n.888G>T | ||
NM_016188.5:c.781G>T MANE Select | NP_057272.1:p.Ala261Ser | |
NR_134539.2:n.875G>T |