HGVS | Genome Assembly |
---|---|
NC_000003.12:g.50345732T>C , CM000665.2:g.50345732T>C | GRCh38 |
NC_000003.11:g.50383163T>C , CM000665.1:g.50383163T>C | GRCh37 |
NC_000003.10:g.50358167T>C | NCBI36 |
NG_023270.1:g.205A>G | |
NG_042828.1:g.5015A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000231749.8:c.-153A>G MANE Select | ENSP00000231749.3:n.-153A>G | |
ENST00000231749.7:c.-153A>G | ENSP00000231749.3:n.-153A>G | |
ENST00000360165.7:c.-153A>G | ENSP00000353289.3:n.-153A>G | |
NM_001308379.1:c.-153A>G | NP_001295308.1:n.-153A>G | |
NM_015896.3:c.-153A>G | NP_056980.2:n.-153A>G | |
XM_005265216.2:c.-281A>G | XP_005265273.1:n.-281A>G | |
NM_015896.4:c.-153A>G MANE Select | NP_056980.2:n.-153A>G | |
NM_001308379.2:c.-153A>G | NP_001295308.1:n.-153A>G |