Canonical Allele Identifier: CA76316045
Gene:

Linked Data

dbSNP Id: rs973169369
MyVariant Identifiers: chr3:g.61413686C>A (hg19) chr3:g.61428012C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428012C>A , CM000665.2:g.61428012C>A GRCh38
NC_000003.11:g.61413686C>A , CM000665.1:g.61413686C>A GRCh37
NC_000003.10:g.61388726C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.165-326G>T
XR_940893.1:n.164+502G>T
XR_001740725.1:n.202+502G>T
XR_940892.2:n.203-326G>T
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