Canonical Allele Identifier: CA2512193807
Gene: DGCR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19059084C>T , CM000684.2:g.19059084C>T GRCh38
NC_000022.10:g.19046597C>T , CM000684.1:g.19046597C>T GRCh37
NC_000022.9:g.17426597C>T NCBI36
NG_021333.1:g.68371G>A
NG_021333.2:g.68371G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263196.12:c.626-1922G>A MANE Select ENSP00000263196.7:n.626-1922G>A
ENST00000263196.11:c.626-1922G>A ENSP00000263196.7:n.626-1922G>A
ENST00000389262.8:c.-48+1482G>A ENSP00000373914.4:n.-48+1482G>A
ENST00000473832.1:n.438-1922G>A
ENST00000537045.5:c.503-1922G>A ENSP00000440062.1:n.503-1922G>A
ENST00000545799.5:c.626-1922G>A ENSP00000445069.2:n.626-1922G>A
ENST00000608548.1:n.77-1922G>A
ENST00000615747.1:c.626-1922G>A ENSP00000482494.1:n.626-1922G>A
NM_001173533.1:c.503-1922G>A NP_001167004.1:n.503-1922G>A
NM_001173534.1:c.494-1922G>A NP_001167005.1:n.494-1922G>A
NM_001184781.1:c.617-1922G>A NP_001171710.1:n.617-1922G>A
NM_005137.2:c.626-1922G>A NP_005128.1:n.626-1922G>A
NR_033674.1:n.759-1922G>A
XR_001755405.1:n.874-1922G>A
XR_001755406.2:n.823-1922G>A
NM_005137.3:c.626-1922G>A MANE Select NP_005128.1:n.626-1922G>A
NM_001173534.2:c.494-1922G>A NP_001167005.1:n.494-1922G>A
NM_001184781.2:c.617-1922G>A NP_001171710.1:n.617-1922G>A
NR_033674.2:n.717-1922G>A
NM_001173533.2:c.503-1922G>A NP_001167004.1:n.503-1922G>A