HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570060G>A , CM000664.2:g.149570060G>A | GRCh38 |
NC_000002.11:g.150426574G>A , CM000664.1:g.150426574G>A | GRCh37 |
NC_000002.10:g.150134820G>A | NCBI36 |
NG_009189.1:g.22757C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.805C>T MANE Select | ENSP00000301920.5:p.Leu269Phe | |
ENST00000303319.9:c.805C>T | ENSP00000301920.5:p.Leu269Phe | |
ENST00000422782.2:c.907C>T | ENSP00000408331.2:p.Leu303Phe | |
ENST00000428879.5:c.805C>T | ENSP00000389060.1:p.Leu269Phe | |
NM_015702.2:c.805C>T | NP_056517.1:p.Leu269Phe | |
NM_015702.3:c.805C>T MANE Select | NP_056517.1:p.Leu269Phe |