Canonical Allele Identifier: CA2395698186
Gene: DGCR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19059090G= , CM000684.2:g.19059090G= GRCh38
NC_000022.10:g.19046603G= , CM000684.1:g.19046603G= GRCh37
NC_000022.9:g.17426603G= NCBI36
NG_021333.1:g.68365C=
NG_021333.2:g.68365C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263196.12:c.626-1928C= MANE Select ENSP00000263196.7:n.626-1928C=
ENST00000263196.11:c.626-1928C= ENSP00000263196.7:n.626-1928C=
ENST00000389262.8:c.-48+1476C= ENSP00000373914.4:n.-48+1476C=
ENST00000473832.1:n.438-1928C=
ENST00000537045.5:c.503-1928C= ENSP00000440062.1:n.503-1928C=
ENST00000545799.5:c.626-1928C= ENSP00000445069.2:n.626-1928C=
ENST00000608548.1:n.77-1928C=
ENST00000615747.1:c.626-1928C= ENSP00000482494.1:n.626-1928C=
NM_001173533.1:c.503-1928C= NP_001167004.1:n.503-1928C=
NM_001173534.1:c.494-1928C= NP_001167005.1:n.494-1928C=
NM_001184781.1:c.617-1928C= NP_001171710.1:n.617-1928C=
NM_005137.2:c.626-1928C= NP_005128.1:n.626-1928C=
NR_033674.1:n.759-1928C=
XR_001755405.1:n.874-1928C=
XR_001755406.2:n.823-1928C=
NM_005137.3:c.626-1928C= MANE Select NP_005128.1:n.626-1928C=
NM_001173534.2:c.494-1928C= NP_001167005.1:n.494-1928C=
NM_001184781.2:c.617-1928C= NP_001171710.1:n.617-1928C=
NR_033674.2:n.717-1928C=
NM_001173533.2:c.503-1928C= NP_001167004.1:n.503-1928C=