Canonical Allele Identifier: CA1462694288
Gene:

Linked Data

dbSNP Id: rs1577991018

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558242C>G , CM000666.2:g.62558242C>G GRCh38
NC_000004.11:g.63423960C>G , CM000666.1:g.63423960C>G GRCh37
NC_000004.10:g.63106555C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5602C>G