Canonical Allele Identifier: CA837065884

Gene:

Linked Data

• dbSNP Id: rs1242097955
• MyVariant Identifiers: chr7:g.26008061G>T (hg19) ; chr7:g.25968441G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.25968441G>T , CM000669.2:g.25968441G>T	GRCh38
NC_000007.13:g.26008061G>T , CM000669.1:g.26008061G>T	GRCh37
NC_000007.12:g.25974586G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927113.1:n.1492-12942C>A
XR_927114.1:n.1492-28980C>A
XR_927115.1:n.1583-12942C>A
XR_927116.1:n.983-12942C>A
XR_927117.1:n.1336-12942C>A
XR_927118.1:n.1580-12942C>A
XR_927119.1:n.1243-12942C>A
XR_927120.1:n.1228-28980C>A
XR_927122.1:n.718-28980C>A
XR_927123.1:n.1201-12942C>A
XR_927113.2:n.1519-12942C>A
XR_927114.2:n.1519-28980C>A
XR_927116.2:n.1013-12942C>A
XR_927117.2:n.1364-12942C>A
XR_927119.2:n.1850-12942C>A
XR_927120.2:n.1256-28980C>A
XR_927122.2:n.750-28980C>A
XR_927123.2:n.1224-12942C>A