HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570104A>T , CM000664.2:g.149570104A>T | GRCh38 |
NC_000002.11:g.150426618A>T , CM000664.1:g.150426618A>T | GRCh37 |
NC_000002.10:g.150134864A>T | NCBI36 |
NG_009189.1:g.22713T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.761T>A MANE Select | ENSP00000301920.5:p.Phe254Tyr | |
ENST00000303319.9:c.761T>A | ENSP00000301920.5:p.Phe254Tyr | |
ENST00000422782.2:c.863T>A | ENSP00000408331.2:p.Phe288Tyr | |
ENST00000428879.5:c.761T>A | ENSP00000389060.1:p.Phe254Tyr | |
NM_015702.2:c.761T>A | NP_056517.1:p.Phe254Tyr | |
NM_015702.3:c.761T>A MANE Select | NP_056517.1:p.Phe254Tyr |