HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86647812T>A , CM000670.2:g.86647812T>A | GRCh38 |
NC_000008.10:g.87660040T>A , CM000670.1:g.87660040T>A | GRCh37 |
NC_000008.9:g.87729156T>A | NCBI36 |
NG_016980.1:g.100864A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.979A>T MANE Select | ENSP00000316605.5:p.Arg327Trp | |
ENST00000681546.1:n.799A>T | ||
ENST00000681746.1:c.979A>T | ENSP00000505959.1:p.Arg327Trp | |
ENST00000320005.5:c.979A>T | ENSP00000316605.5:p.Arg327Trp | |
NM_019098.4:c.979A>T | NP_061971.3:p.Arg327Trp | |
XM_011517138.1:c.565A>T | XP_011515440.1:p.Arg189Trp | |
XM_011517138.2:c.565A>T | XP_011515440.1:p.Arg189Trp | |
NM_019098.5:c.979A>T MANE Select | NP_061971.3:p.Arg327Trp |