Canonical Allele Identifier: CA1087811451

Gene: SNRPC

Linked Data

• dbSNP Id: rs987175022
• gnomAD v3: 6-34762531-CT-C
• gnomAD v4: 6-34762531-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762534del , CM000668.2:g.34762534del	GRCh38
NC_000006.11:g.34730311del , CM000668.1:g.34730311del	GRCh37
NC_000006.10:g.34838289del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244520.10:c.52-61del MANE Select	ENSP00000244520.5:n.52-61del
ENST00000244520.9:c.52-61del	ENSP00000244520.5:n.52-61del
ENST00000374017.3:c.115-61del	ENSP00000363129.3:n.115-61del
ENST00000374018.5:c.-72-61del	ENSP00000363130.1:n.-72-61del
ENST00000474635.1:n.44-61del
NM_003093.2:c.52-61del	NP_003084.1:n.52-61del
NR_029472.1:n.459-61del
NM_003093.3:c.52-61del MANE Select	NP_003084.1:n.52-61del
NR_029472.2:n.48-61del