Canonical Allele Identifier: CA156301716

Gene:

Linked Data

• dbSNP Id: rs889350086
• MyVariant Identifiers: chr7:g.26645347C>T (hg19) ; chr7:g.26605728C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26605728C>T , CM000669.2:g.26605728C>T	GRCh38
NC_000007.13:g.26645347C>T , CM000669.1:g.26645347C>T	GRCh37
NC_000007.12:g.26611872C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927131.1:n.1118-6358G>A
XR_927131.2:n.1186-6358G>A