Canonical Allele Identifier: CA682822616
Gene:

Linked Data

dbSNP Id: rs1223556440
MyVariant Identifiers: chr12:g.102895121G>A (hg19) chr12:g.102501343G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501343G>A , CM000674.2:g.102501343G>A GRCh38
NC_000012.11:g.102895121G>A , CM000674.1:g.102895121G>A GRCh37
NC_000012.10:g.101419251G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17455G>A
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