Canonical Allele Identifier: CA1118842607
Gene:

Linked Data

dbSNP Id: rs546715387

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125474192A>G , CM000670.2:g.125474192A>G GRCh38
NC_000008.10:g.126486434A>G , CM000670.1:g.126486434A>G GRCh37
NC_000008.9:g.126555616A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+878A>G