Canonical Allele Identifier: CA77076780
Gene:

Linked Data

dbSNP Id: rs1022327086
MyVariant Identifiers: chr3:g.70626389G>A (hg19) chr3:g.70577238G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577238G>A , CM000665.2:g.70577238G>A GRCh38
NC_000003.11:g.70626389G>A , CM000665.1:g.70626389G>A GRCh37
NC_000003.10:g.70709079G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.406+1280C>T
XR_001740559.1:n.366+1280C>T
Search 100 bp 5'
Search 100 bp 3'