HGVS | Genome Assembly |
---|---|
NC_000008.11:g.16992703T>C , CM000670.2:g.16992703T>C | GRCh38 |
NC_000008.10:g.16850212T>C , CM000670.1:g.16850212T>C | GRCh37 |
NC_000008.9:g.16894583T>C | NCBI36 |
NG_015978.1:g.14463A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000180166.6:c.*369A>G MANE Select | ENSP00000180166.5:n.*369A>G | |
ENST00000180166.5:c.*369A>G | ENSP00000180166.5:n.*369A>G | |
NM_019851.3:c.*369A>G MANE Select | NP_062825.1:n.*369A>G |