Canonical Allele Identifier: CA459028472
Gene: DLGAP2 HGNC NCBI

Linked Data

gnomAD v4: 8-1296039-G-T
MyVariant Identifiers: chr8:g.1244299G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1296039G>T , CM000670.2:g.1296039G>T GRCh38
NC_000008.10:g.1244299G>T , CM000670.1:g.1244299G>T GRCh37
NC_000008.9:g.1231706G>T NCBI36
NG_009409.2:g.563321G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000421627.7:c.103+37156G>T ENSP00000400258.3:n.103+37156G>T
ENST00000637795.2:c.106+37156G>T MANE Select ENSP00000489774.1:n.106+37156G>T
NR_111948.1:n.3044C>A
XM_011534761.1:c.-135+37156G>T XP_011533063.1:n.-135+37156G>T
XM_011534762.1:c.-135+37156G>T XP_011533064.1:n.-135+37156G>T
NM_001346810.1:c.106+37156G>T NP_001333739.1:n.106+37156G>T
NM_001346810.2:c.106+37156G>T MANE Select NP_001333739.1:n.106+37156G>T