HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118952831T>C , CM000670.2:g.118952831T>C | GRCh38 |
NC_000008.10:g.119965070T>C , CM000670.1:g.119965070T>C | GRCh37 |
NC_000008.9:g.120034251T>C | NCBI36 |
NG_012202.1:g.4314A>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_005250756.2:c.-60+453T>C | XP_005250813.1:n.-60+453T>C | |
NM_001324095.1:c.-324+453T>C | NP_001311024.1:n.-324+453T>C | |
XM_005250756.3:c.-60+453T>C | XP_005250813.1:n.-60+453T>C | |
NM_001324095.2:c.-324+453T>C | NP_001311024.1:n.-324+453T>C |