Canonical Allele Identifier: CA14751569
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.17141948A>G , CM000682.2:g.17141948A>G GRCh38
NC_000020.10:g.17122593A>G , CM000682.1:g.17122593A>G GRCh37
NC_000020.9:g.17070593A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937288.1:n.310+6816A>G
XR_937289.1:n.310+6816A>G
XR_937288.2:n.310+6816A>G