HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1414750G>T , CM000667.2:g.1414750G>T | GRCh38 |
NC_000005.9:g.1414865G>T , CM000667.1:g.1414865G>T | GRCh37 |
NC_000005.8:g.1467865G>T | NCBI36 |
NG_015885.1:g.35679C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.1097C>A MANE Select | ENSP00000270349.9:p.Ser366Tyr | |
ENST00000270349.11:c.1097C>A | ENSP00000270349.9:p.Ser366Tyr | |
ENST00000511750.1:n.547C>A | ||
NM_001044.4:c.1097C>A | NP_001035.1:p.Ser366Tyr | |
NM_001044.5:c.1097C>A MANE Select | NP_001035.1:p.Ser366Tyr |