Canonical Allele Identifier: CA909861276
Gene:

Linked Data

dbSNP Id: rs1005673503
MyVariant Identifiers: chr3:g.70626377G>A (hg19) chr3:g.70577226G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577226G>A , CM000665.2:g.70577226G>A GRCh38
NC_000003.11:g.70626377G>A , CM000665.1:g.70626377G>A GRCh37
NC_000003.10:g.70709067G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940947.1:n.407-1273C>T
XR_001740559.1:n.367-1273C>T
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Search 100 bp 3'