Canonical Allele Identifier: CA817908523
Gene:

Linked Data

dbSNP Id: rs1380369799
MyVariant Identifiers: chr6:g.11943785G>A (hg19) chr6:g.11943552G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943552G>A , CM000668.2:g.11943552G>A GRCh38
NC_000006.11:g.11943785G>A , CM000668.1:g.11943785G>A GRCh37
NC_000006.10:g.12051771G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7983G>A
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