HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129813786G>A , CM000671.2:g.129813786G>A | GRCh38 |
NC_000009.11:g.132576065G>A , CM000671.1:g.132576065G>A | GRCh37 |
NC_000009.10:g.131615886G>A | NCBI36 |
NG_008049.1:g.15377C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.*186C>T MANE Select | ENSP00000345719.4:n.*186C>T | |
ENST00000651202.1:c.*453C>T | ENSP00000498222.1:n.*453C>T | |
ENST00000351698.4:c.*186C>T | ENSP00000345719.4:n.*186C>T | |
ENST00000474192.1:n.769C>T | ||
NM_000113.2:c.*186C>T | NP_000104.1:n.*186C>T | |
XR_929731.3:n.1380C>T | ||
NM_000113.3:c.*186C>T MANE Select | NP_000104.1:n.*186C>T |