Canonical Allele Identifier: CA1687324626
Gene:

Linked Data

dbSNP Id: rs1782267770

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9816849G>C , CM000669.2:g.9816849G>C GRCh38
NC_000007.13:g.9856478G>C , CM000669.1:g.9856478G>C GRCh37
NC_000007.12:g.9823003G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927024.1:n.209+49941C>G
XR_927025.1:n.323+49941C>G
XR_927026.1:n.209+49941C>G
XR_927026.2:n.209+49941C>G