HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47403025G>T , CM000664.2:g.47403025G>T | GRCh38 |
NC_000002.11:g.47630164G>T , CM000664.1:g.47630164G>T | GRCh37 |
NC_000002.10:g.47483668G>T | NCBI36 |
NG_007110.2:g.4902G>T , LRG_218:g.4902G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233146.6:c.-167G>T | ENSP00000233146.2:n.-167G>T |