Canonical Allele Identifier: CA2059284995
Gene:

Linked Data

dbSNP Id: rs1566017403
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501335A>G , CM000674.2:g.102501335A>G GRCh38
NC_000012.11:g.102895113A>G , CM000674.1:g.102895113A>G GRCh37
NC_000012.10:g.101419243A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17447A>G
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