HGVS | Genome Assembly |
---|---|
NC_000011.10:g.72134552T>C , CM000673.2:g.72134552T>C | GRCh38 |
NC_000011.9:g.71845598T>C , CM000673.1:g.71845598T>C | GRCh37 |
NC_000011.8:g.71523246T>C | NCBI36 |
NG_032935.1:g.3828T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622388.4:c.-6-1395T>C | ENSP00000481833.1:n.-6-1395T>C |