HGVS | Genome Assembly |
---|---|
NC_000009.12:g.137199316C>T , CM000671.2:g.137199316C>T | GRCh38 |
NC_000009.11:g.140093768C>T , CM000671.1:g.140093768C>T | GRCh37 |
NC_000009.10:g.139213589C>T | NCBI36 |
NG_027801.1:g.6396G>A | |
NG_027801.2:g.9878G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409012.6:c.1396G>A MANE Select | ENSP00000387100.4:p.Ala466Thr | |
ENST00000333046.8:c.790G>A | ENSP00000327617.4:p.Ala264Thr | |
ENST00000409012.4:c.1396G>A | ENSP00000387100.4:p.Ala466Thr | |
ENST00000541945.1:n.90+4788G>A | ||
NM_001128228.2:c.1396G>A | NP_001121700.2:p.Ala466Thr | |
NM_001128228.3:c.1396G>A MANE Select | NP_001121700.2:p.Ala466Thr |