HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24956827T>G , CM000670.2:g.24956827T>G | GRCh38 |
NC_000008.10:g.24814341T>G , CM000670.1:g.24814341T>G | GRCh37 |
NC_000008.9:g.24870258T>G | NCBI36 |
NG_008492.1:g.4791A>C , LRG_259:g.4791A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.1:c.-312A>C | ENSP00000482169.1:n.-312A>C | |
NM_006158.4:c.-312A>C , LRG_259t1:c.-312A>C | NP_006149.2:n.-312A>C |