HGVS | Genome Assembly |
---|---|
NC_000004.12:g.35981489C>T , CM000666.2:g.35981489C>T | GRCh38 |
NC_000004.11:g.35983111C>T , CM000666.1:g.35983111C>T | GRCh37 |
NC_000004.10:g.35659506C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000503225.5:n.1607+3741G>A | ||
XR_925192.1:n.1460G>A |