Canonical Allele Identifier: CA13993796
Gene: SYNE2 HGNC NCBI

Linked Data

dbSNP Id: rs17101394
gnomAD v2: 14-64232386-G-A
gnomAD v3: 14-63765668-G-A
gnomAD v4: 14-63765668-G-A
MyVariant Identifiers: chr14:g.64232386G>A (hg19) chr14:g.63765668G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.63765668G>A , CM000676.2:g.63765668G>A GRCh38
NC_000014.8:g.64232386G>A , CM000676.1:g.64232386G>A GRCh37
NC_000014.7:g.63302139G>A NCBI36
NG_011756.2:g.8770G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000674003.1:c.-305+3682G>A ENSP00000501132.1:n.-305+3682G>A
XM_011536576.2:c.-305+3682G>A XP_011534878.1:n.-305+3682G>A
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