Canonical Allele Identifier: CA832742536
Gene:

Linked Data

dbSNP Id: rs1213419253
gnomAD v3: 7-124306423-C-A
gnomAD v4: 7-124306423-C-A
MyVariant Identifiers: chr7:g.123946477C>A (hg19) chr7:g.124306423C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306423C>A , CM000669.2:g.124306423C>A GRCh38
NC_000007.13:g.123946477C>A , CM000669.1:g.123946477C>A GRCh37
NC_000007.12:g.123733713C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-55C>A
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Search 100 bp 3'