HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570030T>A , CM000664.2:g.149570030T>A | GRCh38 |
NC_000002.11:g.150426544T>A , CM000664.1:g.150426544T>A | GRCh37 |
NC_000002.10:g.150134790T>A | NCBI36 |
NG_009189.1:g.22787A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.835A>T MANE Select | ENSP00000301920.5:p.Ile279Phe | |
ENST00000303319.9:c.835A>T | ENSP00000301920.5:p.Ile279Phe | |
ENST00000422782.2:c.937A>T | ENSP00000408331.2:p.Ile313Phe | |
ENST00000428879.5:c.835A>T | ENSP00000389060.1:p.Ile279Phe | |
NM_015702.2:c.835A>T | NP_056517.1:p.Ile279Phe | |
NM_015702.3:c.835A>T MANE Select | NP_056517.1:p.Ile279Phe |