HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24956713T>C , CM000670.2:g.24956713T>C | GRCh38 |
NC_000008.10:g.24814227T>C , CM000670.1:g.24814227T>C | GRCh37 |
NC_000008.9:g.24870144T>C | NCBI36 |
NG_008492.1:g.4905A>G , LRG_259:g.4905A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.1:c.-198A>G | ENSP00000482169.1:n.-198A>G | |
ENST00000615973.1:n.9A>G | ||
NM_006158.4:c.-198A>G , LRG_259t1:c.-198A>G | NP_006149.2:n.-198A>G |