Canonical Allele Identifier: CA707666409

Gene: SYNE2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.63809094T>A , CM000676.2:g.63809094T>A	GRCh38
NC_000014.8:g.64275812T>A , CM000676.1:g.64275812T>A	GRCh37
NC_000014.7:g.63345565T>A	NCBI36
NG_011756.2:g.52196T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674003.1:c.-304-43407T>A	ENSP00000501132.1:n.-304-43407T>A
XM_011536576.2:c.-304-43407T>A	XP_011534878.1:n.-304-43407T>A