HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129813810C>A , CM000671.2:g.129813810C>A | GRCh38 |
NC_000009.11:g.132576089C>A , CM000671.1:g.132576089C>A | GRCh37 |
NC_000009.10:g.131615910C>A | NCBI36 |
NG_008049.1:g.15353G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000351698.5:c.*162G>T MANE Select | ENSP00000345719.4:n.*162G>T | |
ENST00000651202.1:c.*429G>T | ENSP00000498222.1:n.*429G>T | |
ENST00000351698.4:c.*162G>T | ENSP00000345719.4:n.*162G>T | |
ENST00000474192.1:n.745G>T | ||
NM_000113.2:c.*162G>T | NP_000104.1:n.*162G>T | |
XR_929731.3:n.1356G>T | ||
NM_000113.3:c.*162G>T MANE Select | NP_000104.1:n.*162G>T |