Canonical Allele Identifier: CA909017060
Gene:

Linked Data

dbSNP Id: rs1308434387
MyVariant Identifiers: chr3:g.61413599A>G (hg19) chr3:g.61427925A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61427925A>G , CM000665.2:g.61427925A>G GRCh38
NC_000003.11:g.61413599A>G , CM000665.1:g.61413599A>G GRCh37
NC_000003.10:g.61388639A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.165-239T>C
XR_940893.1:n.164+589T>C
XR_001740725.1:n.202+589T>C
XR_940892.2:n.203-239T>C
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