HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47783025C>A , CM000664.2:g.47783025C>A | GRCh38 |
NC_000002.11:g.48010164C>A , CM000664.1:g.48010164C>A | GRCh37 |
NC_000002.10:g.47863668C>A | NCBI36 |
NG_007111.1:g.4879C>A , LRG_219:g.4879C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000652107.1:c.-37-7902C>A | ENSP00000498629.1:n.-37-7902C>A | |
ENST00000606499.1:c.-37-7902C>A | ENSP00000475605.1:n.-37-7902C>A |