Canonical Allele Identifier: CA321360823

Gene: DGCR2

Linked Data

• dbSNP Id: rs1027415408
• gnomAD v3: 22-19059099-A-G
• gnomAD v4: 22-19059099-A-G
• MyVariant Identifiers: chr22:g.19046612A>G (hg19) ; chr22:g.19059099A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19059099A>G , CM000684.2:g.19059099A>G	GRCh38
NC_000022.10:g.19046612A>G , CM000684.1:g.19046612A>G	GRCh37
NC_000022.9:g.17426612A>G	NCBI36
NG_021333.1:g.68356T>C
NG_021333.2:g.68356T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263196.12:c.626-1937T>C MANE Select	ENSP00000263196.7:n.626-1937T>C
ENST00000263196.11:c.626-1937T>C	ENSP00000263196.7:n.626-1937T>C
ENST00000389262.8:c.-48+1467T>C	ENSP00000373914.4:n.-48+1467T>C
ENST00000473832.1:n.438-1937T>C
ENST00000537045.5:c.503-1937T>C	ENSP00000440062.1:n.503-1937T>C
ENST00000545799.5:c.626-1937T>C	ENSP00000445069.2:n.626-1937T>C
ENST00000608548.1:n.77-1937T>C
ENST00000615747.1:c.626-1937T>C	ENSP00000482494.1:n.626-1937T>C
NM_001173533.1:c.503-1937T>C	NP_001167004.1:n.503-1937T>C
NM_001173534.1:c.494-1937T>C	NP_001167005.1:n.494-1937T>C
NM_001184781.1:c.617-1937T>C	NP_001171710.1:n.617-1937T>C
NM_005137.2:c.626-1937T>C	NP_005128.1:n.626-1937T>C
NR_033674.1:n.759-1937T>C
XR_001755405.1:n.874-1937T>C
XR_001755406.2:n.823-1937T>C
NM_005137.3:c.626-1937T>C MANE Select	NP_005128.1:n.626-1937T>C
NM_001173534.2:c.494-1937T>C	NP_001167005.1:n.494-1937T>C
NM_001184781.2:c.617-1937T>C	NP_001171710.1:n.617-1937T>C
NR_033674.2:n.717-1937T>C
NM_001173533.2:c.503-1937T>C	NP_001167004.1:n.503-1937T>C