HGVS | Genome Assembly |
---|---|
NC_000016.10:g.72722214T>C , CM000678.2:g.72722214T>C | GRCh38 |
NC_000016.9:g.72756113T>C , CM000678.1:g.72756113T>C | GRCh37 |
NC_000016.8:g.71313614T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XM_017023920.1:c.581+8798T>C | XP_016879409.1:n.581+8798T>C | |
NR_171702.1:n.328+8225T>C | ||
NR_171703.1:n.285+8798T>C | ||
NR_171704.1:n.285+8798T>C | ||
NR_171705.1:n.202-23191T>C |