HGVS | Genome Assembly |
---|---|
NC_000004.12:g.39446738A>T , CM000666.2:g.39446738A>T | GRCh38 |
NC_000004.11:g.39448358A>T , CM000666.1:g.39448358A>T | GRCh37 |
NC_000004.10:g.39124753A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000257408.5:c.2012A>T MANE Select | ENSP00000257408.4:p.Gln671Leu | |
ENST00000257408.4:c.2012A>T | ENSP00000257408.4:p.Gln671Leu | |
NM_175737.3:c.2012A>T | NP_783864.1:p.Gln671Leu | |
XM_005262644.1:c.1985A>T | XP_005262701.1:p.Gln662Leu | |
NM_175737.4:c.2012A>T MANE Select | NP_783864.1:p.Gln671Leu |