Canonical Allele Identifier: CA1069675711
Gene:

Linked Data

dbSNP Id: rs1743707784

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.153943634C>A , CM000666.2:g.153943634C>A GRCh38
NC_000004.11:g.154864786C>A , CM000666.1:g.154864786C>A GRCh37
NC_000004.10:g.155084236C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741892.1:n.1348-5187C>A