HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442474G>C , CM000666.2:g.177442474G>C | GRCh38 |
NC_000004.11:g.178363628G>C , CM000666.1:g.178363628G>C | GRCh37 |
NC_000004.10:g.178600622G>C | NCBI36 |
NG_011845.2:g.5030C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264595.6:c.-99C>G | ENSP00000264595.2:n.-99C>G | |
NM_000027.3:c.-99C>G | NP_000018.2:n.-99C>G | |
NM_001171988.1:c.-99C>G | NP_001165459.1:n.-99C>G | |
NR_033655.1:n.30C>G | ||
XM_006714123.2:c.-99C>G | XP_006714186.1:n.-99C>G |