Canonical Allele Identifier: CA566453926
Gene: SNRPC HGNC NCBI

Linked Data

dbSNP Id: rs1468081642
gnomAD v2: 6-34730317-A-AT
gnomAD v3: 6-34762540-A-AT
gnomAD v4: 6-34762540-A-AT
MyVariant Identifiers: chr6:g.34730317_34730318insT (hg19) chr6:g.34762540_34762541insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762545dup , CM000668.2:g.34762545dup GRCh38
NC_000006.11:g.34730322dup , CM000668.1:g.34730322dup GRCh37
NC_000006.10:g.34838300dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.52-50dup MANE Select ENSP00000244520.5:n.52-50dup
ENST00000244520.9:c.52-50dup ENSP00000244520.5:n.52-50dup
ENST00000374017.3:c.115-50dup ENSP00000363129.3:n.115-50dup
ENST00000374018.5:c.-72-50dup ENSP00000363130.1:n.-72-50dup
ENST00000474635.1:n.44-50dup
NM_003093.2:c.52-50dup NP_003084.1:n.52-50dup
NR_029472.1:n.459-50dup
NM_003093.3:c.52-50dup MANE Select NP_003084.1:n.52-50dup
NR_029472.2:n.48-50dup
Search 100 bp 5'
Search 100 bp 3'