Canonical Allele Identifier: CA682822598
Gene:

Linked Data

dbSNP Id: rs1222788140
MyVariant Identifiers: chr12:g.102895107T>C (hg19) chr12:g.102501329T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501329T>C , CM000674.2:g.102501329T>C GRCh38
NC_000012.11:g.102895107T>C , CM000674.1:g.102895107T>C GRCh37
NC_000012.10:g.101419237T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17441T>C
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