Canonical Allele Identifier: CA1715429592
Gene:

Linked Data

dbSNP Id: rs1788207992

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146883C>T , CM000669.2:g.69146883C>T GRCh38
NC_000007.13:g.68611870C>T , CM000669.1:g.68611870C>T GRCh37
NC_000007.12:g.68249806C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-757G>A