Canonical Allele Identifier: CA2142365961
Gene: SYNE2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.63768838G= , CM000676.2:g.63768838G= GRCh38
NC_000014.8:g.64235556G= , CM000676.1:g.64235556G= GRCh37
NC_000014.7:g.63305309G= NCBI36
NG_011756.2:g.11940G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000674003.1:c.-305+6852G= ENSP00000501132.1:n.-305+6852G=
XM_011536576.2:c.-305+6852G= XP_011534878.1:n.-305+6852G=