Canonical Allele Identifier: CA16303442
Gene:

Linked Data

dbSNP Id: rs6945541
gnomAD v2: 7-68611960-C-T
gnomAD v3: 7-69146973-C-T
gnomAD v4: 7-69146973-C-T
MyVariant Identifiers: chr7:g.68611960C>T (hg19) chr7:g.69146973C>T (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146973C>T , CM000669.2:g.69146973C>T GRCh38
NC_000007.13:g.68611960C>T , CM000669.1:g.68611960C>T GRCh37
NC_000007.12:g.68249896C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-847G>A
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