Canonical Allele Identifier: CA1374121626
Gene:

Linked Data

dbSNP Id: rs1704108250
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266850A>T , CM000665.2:g.72266850A>T GRCh38
NC_000003.11:g.72316001A>T , CM000665.1:g.72316001A>T GRCh37
NC_000003.10:g.72398691A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8258T>A
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