HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94762822T>A , CM000672.2:g.94762822T>A | GRCh38 |
NC_000010.10:g.96522579T>A , CM000672.1:g.96522579T>A | GRCh37 |
NC_000010.9:g.96512569T>A | NCBI36 |
NG_008384.2:g.5117T>A | |
NG_008384.3:g.5142T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.117T>A MANE Select | ENSP00000360372.3:p.Ile39= | |
ENST00000371321.7:c.117T>A | ENSP00000360372.3:p.Ile39= | |
ENST00000464755.1:c.932-12236T>A | ENSP00000483243.1:n.932-12236T>A | |
ENST00000480405.2:c.117T>A | ENSP00000483847.1:p.Ile39= | |
NM_000769.2:c.117T>A | NP_000760.1:p.Ile39= | |
NM_000769.4:c.117T>A MANE Select | NP_000760.1:p.Ile39= |