Canonical Allele Identifier: CA837065814

Gene:

Linked Data

• dbSNP Id: rs1394069503
• gnomAD v3: 7-25968359-C-T
• gnomAD v4: 7-25968359-C-T
• MyVariant Identifiers: chr7:g.26007979C>T (hg19) ; chr7:g.25968359C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.25968359C>T , CM000669.2:g.25968359C>T	GRCh38
NC_000007.13:g.26007979C>T , CM000669.1:g.26007979C>T	GRCh37
NC_000007.12:g.25974504C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927113.1:n.1492-12860G>A
XR_927114.1:n.1492-28898G>A
XR_927115.1:n.1583-12860G>A
XR_927116.1:n.983-12860G>A
XR_927117.1:n.1336-12860G>A
XR_927118.1:n.1580-12860G>A
XR_927119.1:n.1243-12860G>A
XR_927120.1:n.1228-28898G>A
XR_927122.1:n.718-28898G>A
XR_927123.1:n.1201-12860G>A
XR_927113.2:n.1519-12860G>A
XR_927114.2:n.1519-28898G>A
XR_927116.2:n.1013-12860G>A
XR_927117.2:n.1364-12860G>A
XR_927119.2:n.1850-12860G>A
XR_927120.2:n.1256-28898G>A
XR_927122.2:n.750-28898G>A
XR_927123.2:n.1224-12860G>A