Canonical Allele Identifier: CA15535859
Gene:

Linked Data

dbSNP Id: rs2106595
gnomAD v2: 7-118159549-G-A
gnomAD v3: 7-118519495-G-A
gnomAD v4: 7-118519495-G-A
MyVariant Identifiers: chr7:g.118159549G>A (hg19) chr7:g.118519495G>A (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.118519495G>A , CM000669.2:g.118519495G>A GRCh38
NC_000007.13:g.118159549G>A , CM000669.1:g.118159549G>A GRCh37
NC_000007.12:g.117946785G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927908.1:n.388+5668G>A
XR_927909.1:n.388+5668G>A
XR_927910.1:n.388+5668G>A
XR_927909.2:n.426+5668G>A
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