Canonical Allele Identifier: CA797158722
Gene:

Linked Data

dbSNP Id: rs1388869184

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558294A>G , CM000666.2:g.62558294A>G GRCh38
NC_000004.11:g.63424012A>G , CM000666.1:g.63424012A>G GRCh37
NC_000004.10:g.63106607A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5550A>G