HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570118G>C , CM000664.2:g.149570118G>C | GRCh38 |
NC_000002.11:g.150426632G>C , CM000664.1:g.150426632G>C | GRCh37 |
NC_000002.10:g.150134878G>C | NCBI36 |
NG_009189.1:g.22699C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000303319.10:c.747C>G MANE Select | ENSP00000301920.5:p.Tyr249Ter | |
ENST00000303319.9:c.747C>G | ENSP00000301920.5:p.Tyr249Ter | |
ENST00000422782.2:c.849C>G | ENSP00000408331.2:p.Tyr283Ter | |
ENST00000428879.5:c.747C>G | ENSP00000389060.1:p.Tyr249Ter | |
NM_015702.2:c.747C>G | NP_056517.1:p.Tyr249Ter | |
NM_015702.3:c.747C>G MANE Select | NP_056517.1:p.Tyr249Ter |