HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75009087G>T , CM000676.2:g.75009087G>T | GRCh38 |
NC_000014.8:g.75475790G>T , CM000676.1:g.75475790G>T | GRCh37 |
NC_000014.7:g.74545543G>T | NCBI36 |
NG_013333.1:g.11179G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.955G>T MANE Select | ENSP00000266126.5:p.Glu319Ter | |
ENST00000266126.9:c.955G>T | ENSP00000266126.5:p.Glu319Ter | |
ENST00000556668.1:n.535G>T | ||
NM_014239.3:c.955G>T | NP_055054.1:p.Glu319Ter | |
NM_014239.4:c.955G>T MANE Select | NP_055054.1:p.Glu319Ter |