Canonical Allele Identifier: CA11988280
Gene: TENM2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2937573

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.167044193G>A , CM000667.2:g.167044193G>A GRCh38
NC_000005.8:g.166403776G>A NCBI36
NC_000005.9:g.166471198G>A , CM000667.1:g.166471198G>A GRCh37

Transcript Alleles

HGVS Amino-acid change
XM_005265950.1:c.-189-29049G>A XP_005266007.1:p.=
XM_006714897.1:c.-189-29049G>A XP_006714960.1:p.=
XM_011534604.1:c.-189-29049G>A XP_011532906.1:p.=