Canonical Allele Identifier: CA837065741
Gene:

Linked Data

dbSNP Id: rs1454214328
gnomAD v3: 7-25968239-A-C
gnomAD v4: 7-25968239-A-C
MyVariant Identifiers: chr7:g.26007859A>C (hg19) chr7:g.25968239A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.25968239A>C , CM000669.2:g.25968239A>C GRCh38
NC_000007.13:g.26007859A>C , CM000669.1:g.26007859A>C GRCh37
NC_000007.12:g.25974384A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927113.1:n.1492-12740T>G
XR_927114.1:n.1492-28778T>G
XR_927115.1:n.1583-12740T>G
XR_927116.1:n.983-12740T>G
XR_927117.1:n.1336-12740T>G
XR_927118.1:n.1580-12740T>G
XR_927119.1:n.1243-12740T>G
XR_927120.1:n.1228-28778T>G
XR_927122.1:n.718-28778T>G
XR_927123.1:n.1201-12740T>G
XR_927113.2:n.1519-12740T>G
XR_927114.2:n.1519-28778T>G
XR_927116.2:n.1013-12740T>G
XR_927117.2:n.1364-12740T>G
XR_927119.2:n.1850-12740T>G
XR_927120.2:n.1256-28778T>G
XR_927122.2:n.750-28778T>G
XR_927123.2:n.1224-12740T>G
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