HGVS | Genome Assembly |
---|---|
NC_000004.12:g.121697006G>C , CM000666.2:g.121697006G>C | GRCh38 |
NC_000004.11:g.122618161G>C , CM000666.1:g.122618161G>C | GRCh37 |
NC_000004.10:g.122837611G>C | NCBI36 |
NG_032042.1:g.4987C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296511.9:c.-179C>G | ENSP00000296511.5:n.-179C>G |