Canonical Allele Identifier: CA705306358
Gene:

Linked Data

dbSNP Id: rs1281217148
gnomAD v3: 14-36384855-T-G
gnomAD v4: 14-36384855-T-G
MyVariant Identifiers: chr14:g.36854060T>G (hg19) chr14:g.36384855T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384855T>G , CM000676.2:g.36384855T>G GRCh38
NC_000014.8:g.36854060T>G , CM000676.1:g.36854060T>G GRCh37
NC_000014.7:g.35923811T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12304T>G XP_011535730.1:n.319-12304T>G
XR_943756.1:n.358+23759T>G
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