HGVS | Genome Assembly |
---|---|
NC_000004.12:g.35981395C>G , CM000666.2:g.35981395C>G | GRCh38 |
NC_000004.11:g.35983017C>G , CM000666.1:g.35983017C>G | GRCh37 |
NC_000004.10:g.35659412C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000503225.5:n.1607+3835G>C | ||
XR_925192.1:n.1554G>C |