Canonical Allele Identifier: CA205143430
Gene:

Linked Data

dbSNP Id: rs762512617

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075798C>A , CM000672.2:g.29075798C>A GRCh38
NC_000010.10:g.29364727C>A , CM000672.1:g.29364727C>A GRCh37
NC_000010.9:g.29404733C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3694C>A