Canonical Allele Identifier: CA14202044
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60217977A>G , CM000677.2:g.60217977A>G GRCh38
NC_000015.9:g.60510176A>G , CM000677.1:g.60510176A>G GRCh37
NC_000015.8:g.58297468A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932310.1:n.312-34448A>G
XR_932310.2:n.609-34448A>G