Canonical Allele Identifier: CA682822531
Gene:

Linked Data

dbSNP Id: rs1220408395
MyVariant Identifiers: chr12:g.102895060G>A (hg19) chr12:g.102501282G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501282G>A , CM000674.2:g.102501282G>A GRCh38
NC_000012.11:g.102895060G>A , CM000674.1:g.102895060G>A GRCh37
NC_000012.10:g.101419190G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17394G>A
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