HGVS | Genome Assembly |
---|---|
NC_000005.10:g.174724579T>C , CM000667.2:g.174724579T>C | GRCh38 |
NC_000005.9:g.174151582T>C , CM000667.1:g.174151582T>C | GRCh37 |
NC_000005.8:g.174084188T>C | NCBI36 |
NG_008124.1:g.5008T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239243.6:c.-81T>C | ENSP00000239243.5:n.-81T>C | |
NM_002449.4:c.-81T>C | NP_002440.2:n.-81T>C | |
NM_001363626.1:c.-81T>C | NP_001350555.1:n.-81T>C |