Canonical Allele Identifier: CA1552561717
Gene:

Linked Data

dbSNP Id: rs1428971548

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.66487832C>G , CM000667.2:g.66487832C>G GRCh38
NC_000005.9:g.65783660C>G , CM000667.1:g.65783660C>G GRCh37
NC_000005.8:g.65819416C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948381.1:n.649-49004C>G