HGVS | Genome Assembly |
---|---|
NC_000002.12:g.219060565G>T , CM000664.2:g.219060565G>T | GRCh38 |
NC_000002.11:g.219925287G>T , CM000664.1:g.219925287G>T | GRCh37 |
NC_000002.10:g.219633531G>T | NCBI36 |
NG_016741.1:g.4952C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295731.7:c.-98C>A MANE Select | ENSP00000295731.5:n.-98C>A | |
NM_002181.4:c.-98C>A MANE Select | NP_002172.2:n.-98C>A |