Canonical Allele Identifier: CA824184845

Gene: SNRPC

Linked Data

• dbSNP Id: rs1167078178
• gnomAD v3: 6-34762531-C-T
• gnomAD v4: 6-34762531-C-T
• MyVariant Identifiers: chr6:g.34730308C>T (hg19) ; chr6:g.34762531C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762531C>T , CM000668.2:g.34762531C>T	GRCh38
NC_000006.11:g.34730308C>T , CM000668.1:g.34730308C>T	GRCh37
NC_000006.10:g.34838286C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244520.10:c.52-64C>T MANE Select	ENSP00000244520.5:n.52-64C>T
ENST00000244520.9:c.52-64C>T	ENSP00000244520.5:n.52-64C>T
ENST00000374017.3:c.115-64C>T	ENSP00000363129.3:n.115-64C>T
ENST00000374018.5:c.-72-64C>T	ENSP00000363130.1:n.-72-64C>T
ENST00000474635.1:n.44-64C>T
NM_003093.2:c.52-64C>T	NP_003084.1:n.52-64C>T
NR_029472.1:n.459-64C>T
NM_003093.3:c.52-64C>T MANE Select	NP_003084.1:n.52-64C>T
NR_029472.2:n.48-64C>T