HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570095T>A , CM000664.2:g.149570095T>A | GRCh38 |
NC_000002.11:g.150426609T>A , CM000664.1:g.150426609T>A | GRCh37 |
NC_000002.10:g.150134855T>A | NCBI36 |
NG_009189.1:g.22722A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000303319.10:c.770A>T MANE Select | ENSP00000301920.5:p.Asp257Val | |
ENST00000303319.9:c.770A>T | ENSP00000301920.5:p.Asp257Val | |
ENST00000422782.2:c.872A>T | ENSP00000408331.2:p.Asp291Val | |
ENST00000428879.5:c.770A>T | ENSP00000389060.1:p.Asp257Val | |
NM_015702.2:c.770A>T | NP_056517.1:p.Asp257Val | |
NM_015702.3:c.770A>T MANE Select | NP_056517.1:p.Asp257Val |