HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38753780G>C , CM000664.2:g.38753780G>C | GRCh38 |
NC_000002.11:g.38980922G>C , CM000664.1:g.38980922G>C | GRCh37 |
NC_000002.10:g.38834426G>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000409011.5:c.-281+1962G>C | ENSP00000387191.1:n.-281+1962G>C |