Canonical Allele Identifier: CA259369476
Gene:

Linked Data

dbSNP Id: rs903282363
gnomAD v2: 14-36854027-G-A
gnomAD v3: 14-36384822-G-A
gnomAD v4: 14-36384822-G-A
MyVariant Identifiers: chr14:g.36854027G>A (hg19) chr14:g.36384822G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384822G>A , CM000676.2:g.36384822G>A GRCh38
NC_000014.8:g.36854027G>A , CM000676.1:g.36854027G>A GRCh37
NC_000014.7:g.35923778G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12337G>A XP_011535730.1:n.319-12337G>A
XR_943756.1:n.358+23726G>A
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