Canonical Allele Identifier: CA1462694332
Gene:

Linked Data

dbSNP Id: rs1756230608
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558345A>G , CM000666.2:g.62558345A>G GRCh38
NC_000004.11:g.63424063A>G , CM000666.1:g.63424063A>G GRCh37
NC_000004.10:g.63106658A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5499A>G
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