Canonical Allele Identifier: CA156301715

Gene:

Linked Data

• dbSNP Id: rs935315562
• MyVariant Identifiers: chr7:g.26605727A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26605727A>G , CM000669.2:g.26605727A>G	GRCh38
NC_000007.13:g.26645346A>G , CM000669.1:g.26645346A>G	GRCh37
NC_000007.12:g.26611871A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927131.1:n.1118-6357T>C
XR_927131.2:n.1186-6357T>C