HGVS | Genome Assembly |
---|---|
NC_000004.12:g.87610889T>G , CM000666.2:g.87610889T>G | GRCh38 |
NC_000004.11:g.88532041T>G , CM000666.1:g.88532041T>G | GRCh37 |
NC_000004.10:g.88751065T>G | NCBI36 |
NG_011595.1:g.7361T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651931.1:c.-20T>G MANE Select | ENSP00000498766.1:n.-20T>G | |
ENST00000282478.7:c.-20T>G | ENSP00000282478.7:n.-20T>G | |
ENST00000399271.5:c.-20T>G | ENSP00000382213.1:n.-20T>G | |
NM_014208.3:c.-20T>G MANE Select | NP_055023.2:n.-20T>G |