HGVS | Genome Assembly |
---|---|
NC_000004.12:g.121697013C>A , CM000666.2:g.121697013C>A | GRCh38 |
NC_000004.11:g.122618168C>A , CM000666.1:g.122618168C>A | GRCh37 |
NC_000004.10:g.122837618C>A | NCBI36 |
NG_032042.1:g.4980G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296511.9:c.-186G>T | ENSP00000296511.5:n.-186G>T |