HGVS | Genome Assembly |
---|---|
NC_000011.10:g.62856008A>C , CM000673.2:g.62856008A>C | GRCh38 |
NC_000011.9:g.62623480A>C , CM000673.1:g.62623480A>C | GRCh37 |
NC_000011.8:g.62380056A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680002.1:c.-262A>C | ENSP00000506366.1:n.-262A>C | |
ENST00000680729.1:c.-262A>C | ENSP00000505639.1:n.-262A>C |