HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570159G>T , CM000664.2:g.149570159G>T | GRCh38 |
NC_000002.11:g.150426673G>T , CM000664.1:g.150426673G>T | GRCh37 |
NC_000002.10:g.150134919G>T | NCBI36 |
NG_009189.1:g.22658C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.706C>A MANE Select | ENSP00000301920.5:p.Pro236Thr | |
ENST00000303319.9:c.706C>A | ENSP00000301920.5:p.Pro236Thr | |
ENST00000422782.2:c.808C>A | ENSP00000408331.2:p.Pro270Thr | |
ENST00000428879.5:c.706C>A | ENSP00000389060.1:p.Pro236Thr | |
NM_015702.2:c.706C>A | NP_056517.1:p.Pro236Thr | |
NM_015702.3:c.706C>A MANE Select | NP_056517.1:p.Pro236Thr |