HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135028928T>C , CM000667.2:g.135028928T>C | GRCh38 |
NC_000005.9:g.134364618T>C , CM000667.1:g.134364618T>C | GRCh37 |
NC_000005.8:g.134392517T>C | NCBI36 |
NG_012114.1:g.10347A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.796A>G MANE Select | ENSP00000265340.6:p.Thr266Ala | |
ENST00000265340.11:c.796A>G | ENSP00000265340.6:p.Thr266Ala | |
ENST00000506438.5:c.796A>G | ENSP00000427542.1:p.Thr266Ala | |
NM_002653.4:c.796A>G | NP_002644.4:p.Thr266Ala | |
NM_002653.5:c.796A>G MANE Select | NP_002644.4:p.Thr266Ala |