HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570157T>A , CM000664.2:g.149570157T>A | GRCh38 |
NC_000002.11:g.150426671T>A , CM000664.1:g.150426671T>A | GRCh37 |
NC_000002.10:g.150134917T>A | NCBI36 |
NG_009189.1:g.22660A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.708A>T MANE Select | ENSP00000301920.5:p.Pro236= | |
ENST00000303319.9:c.708A>T | ENSP00000301920.5:p.Pro236= | |
ENST00000422782.2:c.810A>T | ENSP00000408331.2:p.Pro270= | |
ENST00000428879.5:c.708A>T | ENSP00000389060.1:p.Pro236= | |
NM_015702.2:c.708A>T | NP_056517.1:p.Pro236= | |
NM_015702.3:c.708A>T MANE Select | NP_056517.1:p.Pro236= |