HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133644185A>T , CM000671.2:g.133644185A>T | GRCh38 |
NC_000009.11:g.136509307A>T , CM000671.1:g.136509307A>T | GRCh37 |
NC_000009.10:g.135499128A>T | NCBI36 |
NG_008645.1:g.12823A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393056.8:c.922-33A>T MANE Select | ENSP00000376776.2:n.922-33A>T | |
ENST00000393056.6:c.922-33A>T | ENSP00000376776.2:n.922-33A>T | |
NM_000787.3:c.922-33A>T | NP_000778.3:n.922-33A>T | |
NM_000787.4:c.922-33A>T MANE Select | NP_000778.3:n.922-33A>T |