HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24956689C>G , CM000670.2:g.24956689C>G | GRCh38 |
NC_000008.10:g.24814203C>G , CM000670.1:g.24814203C>G | GRCh37 |
NC_000008.9:g.24870120C>G | NCBI36 |
NG_008492.1:g.4929G>C , LRG_259:g.4929G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.1:c.-174G>C | ENSP00000482169.1:n.-174G>C | |
ENST00000615973.1:n.33G>C | ||
NM_006158.4:c.-174G>C , LRG_259t1:c.-174G>C | NP_006149.2:n.-174G>C |