Canonical Allele Identifier: CA156301736

Gene:

Linked Data

• dbSNP Id: rs981886876
• MyVariant Identifiers: chr7:g.26645440T>A (hg19) ; chr7:g.26605821T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26605821T>A , CM000669.2:g.26605821T>A	GRCh38
NC_000007.13:g.26645440T>A , CM000669.1:g.26645440T>A	GRCh37
NC_000007.12:g.26611965T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927131.1:n.1118-6451A>T
XR_927131.2:n.1186-6451A>T