Canonical Allele Identifier: CA363727958

Gene: SNRPC

Linked Data

• MyVariant Identifiers: chr6:g.34730404G>T (hg19) ; chr6:g.34762627G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762627G>T , CM000668.2:g.34762627G>T	GRCh38
NC_000006.11:g.34730404G>T , CM000668.1:g.34730404G>T	GRCh37
NC_000006.10:g.34838382G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244520.10:c.84G>T MANE Select	ENSP00000244520.5:p.Arg28Ser
ENST00000244520.9:c.84G>T	ENSP00000244520.5:p.Arg28Ser
ENST00000374017.3:c.147G>T	ENSP00000363129.3:p.Arg49Ser
ENST00000374018.5:c.-40G>T	ENSP00000363130.1:n.-40G>T
ENST00000474635.1:n.76G>T
NM_003093.2:c.84G>T	NP_003084.1:p.Arg28Ser
NR_029472.1:n.491G>T
NM_003093.3:c.84G>T MANE Select	NP_003084.1:p.Arg28Ser
NR_029472.2:n.80G>T