Canonical Allele Identifier: CA705306372
Gene:

Linked Data

dbSNP Id: rs1297803810
gnomAD v3: 14-36384914-T-C
gnomAD v4: 14-36384914-T-C
MyVariant Identifiers: chr14:g.36854119T>C (hg19) chr14:g.36384914T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384914T>C , CM000676.2:g.36384914T>C GRCh38
NC_000014.8:g.36854119T>C , CM000676.1:g.36854119T>C GRCh37
NC_000014.7:g.35923870T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12245T>C XP_011535730.1:n.319-12245T>C
XR_943756.1:n.358+23818T>C
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