Canonical Allele Identifier: CA166591544
Gene:

Linked Data

dbSNP Id: rs899649429
gnomAD v2: 7-123946415-A-T
gnomAD v3: 7-124306361-A-T
gnomAD v4: 7-124306361-A-T
MyVariant Identifiers: chr7:g.123946415A>T (hg19) chr7:g.124306361A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306361A>T , CM000669.2:g.124306361A>T GRCh38
NC_000007.13:g.123946415A>T , CM000669.1:g.123946415A>T GRCh37
NC_000007.12:g.123733651A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-117A>T
Search 100 bp 5'
Search 100 bp 3'