HGVS | Genome Assembly |
---|---|
NC_000012.12:g.120978365G>C , CM000674.2:g.120978365G>C | GRCh38 |
NC_000012.11:g.121416168G>C , CM000674.1:g.121416168G>C | GRCh37 |
NC_000012.10:g.119900551G>C | NCBI36 |
NG_011731.2:g.4620G>C , LRG_522:g.4620G>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_005253931.2:c.-404G>C | XP_005253988.1:n.-404G>C | |
XM_024449168.1:c.-404G>C | XP_024304936.1:n.-404G>C |