Canonical Allele Identifier: CA1715429697
Gene:

Linked Data

dbSNP Id: rs1584013967

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146941T>C , CM000669.2:g.69146941T>C GRCh38
NC_000007.13:g.68611928T>C , CM000669.1:g.68611928T>C GRCh37
NC_000007.12:g.68249864T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-815A>G