HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102798541G>C , CM000673.2:g.102798541G>C | GRCh38 |
NC_000011.9:g.102669272G>C , CM000673.1:g.102669272G>C | GRCh37 |
NC_000011.8:g.102174482G>C | NCBI36 |
NG_011740.1:g.4695C>G | |
NG_011740.2:g.4695C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371455.7:n.423+419G>C | ||
ENST00000525739.6:n.682+419G>C | ||
ENST00000544704.1:n.443+419G>C | ||
NR_038390.1:n.682+419G>C |