HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570089A>C , CM000664.2:g.149570089A>C | GRCh38 |
NC_000002.11:g.150426603A>C , CM000664.1:g.150426603A>C | GRCh37 |
NC_000002.10:g.150134849A>C | NCBI36 |
NG_009189.1:g.22728T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.776T>G MANE Select | ENSP00000301920.5:p.Leu259Arg | |
ENST00000303319.9:c.776T>G | ENSP00000301920.5:p.Leu259Arg | |
ENST00000422782.2:c.878T>G | ENSP00000408331.2:p.Leu293Arg | |
ENST00000428879.5:c.776T>G | ENSP00000389060.1:p.Leu259Arg | |
NM_015702.2:c.776T>G | NP_056517.1:p.Leu259Arg | |
NM_015702.3:c.776T>G MANE Select | NP_056517.1:p.Leu259Arg |