Canonical Allele Identifier: CA926324480
Gene:

Linked Data

dbSNP Id: rs1835464173

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075718C>A , CM000672.2:g.29075718C>A GRCh38
NC_000010.10:g.29364647C>A , CM000672.1:g.29364647C>A GRCh37
NC_000010.9:g.29404653C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001747284.1:n.127-3774C>A