Canonical Allele Identifier: CA363727953

Gene: SNRPC

Linked Data

• MyVariant Identifiers: chr6:g.34730402A>T (hg19) ; chr6:g.34762625A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762625A>T , CM000668.2:g.34762625A>T	GRCh38
NC_000006.11:g.34730402A>T , CM000668.1:g.34730402A>T	GRCh37
NC_000006.10:g.34838380A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244520.10:c.82A>T MANE Select	ENSP00000244520.5:p.Arg28Trp
ENST00000244520.9:c.82A>T	ENSP00000244520.5:p.Arg28Trp
ENST00000374017.3:c.145A>T	ENSP00000363129.3:p.Arg49Trp
ENST00000374018.5:c.-42A>T	ENSP00000363130.1:n.-42A>T
ENST00000474635.1:n.74A>T
NM_003093.2:c.82A>T	NP_003084.1:p.Arg28Trp
NR_029472.1:n.489A>T
NM_003093.3:c.82A>T MANE Select	NP_003084.1:p.Arg28Trp
NR_029472.2:n.78A>T