Canonical Allele Identifier: CA162129254
Gene:

Linked Data

dbSNP Id: rs1048428936
MyVariant Identifiers: chr7:g.87543101A>T (hg19) chr7:g.87913786A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87913786A>T , CM000669.2:g.87913786A>T GRCh38
NC_000007.13:g.87543101A>T , CM000669.1:g.87543101A>T GRCh37
NC_000007.12:g.87381037A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927723.1:n.148+115T>A
XR_927724.1:n.192+115T>A
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Search 100 bp 3'