HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2444971T>C , CM000673.2:g.2444971T>C | GRCh38 |
NC_000011.9:g.2466201T>C , CM000673.1:g.2466201T>C | GRCh37 |
NC_000011.8:g.2422777T>C | NCBI36 |
NG_008935.1:g.4981T>C , LRG_287:g.4981T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.23+263T>C | ENSP00000434560.2:n.23+263T>C | |
ENST00000496887.6:c.23+263T>C | ENSP00000434560.1:n.23+263T>C |