HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24956772A>C , CM000670.2:g.24956772A>C | GRCh38 |
NC_000008.10:g.24814286A>C , CM000670.1:g.24814286A>C | GRCh37 |
NC_000008.9:g.24870203A>C | NCBI36 |
NG_008492.1:g.4846T>G , LRG_259:g.4846T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.1:c.-257T>G | ENSP00000482169.1:n.-257T>G | |
NM_006158.4:c.-257T>G , LRG_259t1:c.-257T>G | NP_006149.2:n.-257T>G |