HGVS | Genome Assembly |
---|---|
NC_000002.12:g.72891520G>T , CM000664.2:g.72891520G>T | GRCh38 |
NC_000002.11:g.73118649G>T , CM000664.1:g.73118649G>T | GRCh37 |
NC_000002.10:g.72972157G>T | NCBI36 |
NG_008234.1:g.9138G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234454.6:c.769G>T MANE Select | ENSP00000234454.5:p.Asp257Tyr | |
ENST00000234454.5:c.769G>T | ENSP00000234454.5:p.Asp257Tyr | |
ENST00000498749.1:n.714G>T | ||
NM_003124.4:c.769G>T | NP_003115.1:p.Asp257Tyr | |
NM_003124.5:c.769G>T MANE Select | NP_003115.1:p.Asp257Tyr |