Canonical Allele Identifier: CA155958220

Gene:

Linked Data

• dbSNP Id: rs1028350137
• gnomAD v2: 7-26007907-G-C
• gnomAD v3: 7-25968287-G-C
• gnomAD v4: 7-25968287-G-C
• MyVariant Identifiers: chr7:g.26007907G>C (hg19) ; chr7:g.25968287G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.25968287G>C , CM000669.2:g.25968287G>C	GRCh38
NC_000007.13:g.26007907G>C , CM000669.1:g.26007907G>C	GRCh37
NC_000007.12:g.25974432G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927113.1:n.1492-12788C>G
XR_927114.1:n.1492-28826C>G
XR_927115.1:n.1583-12788C>G
XR_927116.1:n.983-12788C>G
XR_927117.1:n.1336-12788C>G
XR_927118.1:n.1580-12788C>G
XR_927119.1:n.1243-12788C>G
XR_927120.1:n.1228-28826C>G
XR_927122.1:n.718-28826C>G
XR_927123.1:n.1201-12788C>G
XR_927113.2:n.1519-12788C>G
XR_927114.2:n.1519-28826C>G
XR_927116.2:n.1013-12788C>G
XR_927117.2:n.1364-12788C>G
XR_927119.2:n.1850-12788C>G
XR_927120.2:n.1256-28826C>G
XR_927122.2:n.750-28826C>G
XR_927123.2:n.1224-12788C>G