Canonical Allele Identifier: CA837079409
Gene:

Linked Data

dbSNP Id: rs1365585199
gnomAD v3: 7-25831394-G-A
gnomAD v4: 7-25831394-G-A
MyVariant Identifiers: chr7:g.25871014G>A (hg19) chr7:g.25831394G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.25831394G>A , CM000669.2:g.25831394G>A GRCh38
NC_000007.13:g.25871014G>A , CM000669.1:g.25871014G>A GRCh37
NC_000007.12:g.25837539G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_108752.3:n.513C>T
XR_927108.1:n.487C>T
XR_927109.1:n.569C>T
XR_927110.1:n.473C>T
XR_108752.4:n.527C>T
XR_927110.2:n.652C>T
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