Canonical Allele Identifier: CA1369169824
Gene:

Linked Data

dbSNP Id: rs1576348672
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428015C>T , CM000665.2:g.61428015C>T GRCh38
NC_000003.11:g.61413689C>T , CM000665.1:g.61413689C>T GRCh37
NC_000003.10:g.61388729C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.165-329G>A
XR_940893.1:n.164+499G>A
XR_001740725.1:n.202+499G>A
XR_940892.2:n.203-329G>A
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