Canonical Allele Identifier: CA909017167
Gene:

Linked Data

dbSNP Id: rs1335705631
MyVariant Identifiers: chr3:g.61413889G>T (hg19) chr3:g.61428215G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428215G>T , CM000665.2:g.61428215G>T GRCh38
NC_000003.11:g.61413889G>T , CM000665.1:g.61413889G>T GRCh37
NC_000003.10:g.61388929G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+299C>A
XR_940893.1:n.164+299C>A
XR_001740725.1:n.202+299C>A
XR_940892.2:n.202+299C>A
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