Canonical Allele Identifier: CA98367604
Gene:

Linked Data

dbSNP Id: rs886526745

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558487G>C , CM000666.2:g.62558487G>C GRCh38
NC_000004.11:g.63424205G>C , CM000666.1:g.63424205G>C GRCh37
NC_000004.10:g.63106800G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5357G>C