HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193122117A>C , CM000663.2:g.193122117A>C | GRCh38 |
NC_000001.10:g.193091247A>C , CM000663.1:g.193091247A>C | GRCh37 |
NC_000001.9:g.191357870A>C | NCBI36 |
NG_012691.1:g.5160A>C , LRG_507:g.5160A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367435.5:c.-84A>C MANE Select | ENSP00000356405.4:n.-84A>C | |
ENST00000643006.1:c.-84A>C | ENSP00000496633.1:n.-84A>C | |
ENST00000649895.1:n.135A>C | ||
ENST00000650197.1:c.-84A>C | ENSP00000496929.1:n.-84A>C | |
ENST00000367435.3:c.-84A>C | ENSP00000356405.3:n.-84A>C | |
NM_024529.4:c.-84A>C , LRG_507t1:c.-84A>C | NP_078805.3:n.-84A>C | |
XM_006711537.2:c.-84A>C | XP_006711600.1:n.-84A>C | |
XM_006711537.4:c.-84A>C | XP_006711600.1:n.-84A>C | |
XR_001738350.1:n.1540T>G | ||
NM_024529.5:c.-84A>C MANE Select | NP_078805.3:n.-84A>C |