Canonical Allele Identifier: CA843440897

Gene:

Linked Data

• dbSNP Id: rs1329977398
• MyVariant Identifiers: chr7:g.87543113A>C (hg19) ; chr7:g.87913798A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87913798A>C , CM000669.2:g.87913798A>C	GRCh38
NC_000007.13:g.87543113A>C , CM000669.1:g.87543113A>C	GRCh37
NC_000007.12:g.87381049A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927723.1:n.148+103T>G
XR_927724.1:n.192+103T>G