Canonical Allele Identifier: CA1462694350
Gene:

Linked Data

dbSNP Id: rs1756231486

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558397T>G , CM000666.2:g.62558397T>G GRCh38
NC_000004.11:g.63424115T>G , CM000666.1:g.63424115T>G GRCh37
NC_000004.10:g.63106710T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5447T>G