Canonical Allele Identifier: CA459028468
Gene: DLGAP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.1244298T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.1296038T>C , CM000670.2:g.1296038T>C GRCh38
NC_000008.10:g.1244298T>C , CM000670.1:g.1244298T>C GRCh37
NC_000008.9:g.1231705T>C NCBI36
NG_009409.2:g.563320T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000421627.7:c.103+37155T>C ENSP00000400258.3:n.103+37155T>C
ENST00000637795.2:c.106+37155T>C MANE Select ENSP00000489774.1:n.106+37155T>C
NR_111948.1:n.3045A>G
XM_011534761.1:c.-135+37155T>C XP_011533063.1:n.-135+37155T>C
XM_011534762.1:c.-135+37155T>C XP_011533064.1:n.-135+37155T>C
NM_001346810.1:c.106+37155T>C NP_001333739.1:n.106+37155T>C
NM_001346810.2:c.106+37155T>C MANE Select NP_001333739.1:n.106+37155T>C
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