Canonical Allele Identifier: CA170278757
Gene: DLGAP2 HGNC NCBI

Linked Data

dbSNP Id: rs10101376
MyVariant Identifiers: chr8:g.1296114A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1296114A>G , CM000670.2:g.1296114A>G GRCh38
NG_009409.2:g.563396A>G

Transcript Alleles

HGVS Amino-acid change
XM_011534761.1:c.-135+37231A>G XP_011533063.1:p.=
XM_011534762.1:c.-135+37231A>G XP_011533064.1:p.=
NM_001346810.1:c.106+37231A>G NP_001333739.1:p.=
NM_001346810.2:c.106+37231A>G MANE Select NP_001333739.1:p.=