Canonical Allele Identifier: CA449892540

Gene: SNRPC

Linked Data

• MyVariant Identifiers: chr6:g.34730458T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762681T>G , CM000668.2:g.34762681T>G	GRCh38
NC_000006.11:g.34730458T>G , CM000668.1:g.34730458T>G	GRCh37
NC_000006.10:g.34838436T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244520.10:c.138T>G MANE Select	ENSP00000244520.5:p.Ala46=
ENST00000244520.9:c.138T>G	ENSP00000244520.5:p.Ala46=
ENST00000374017.3:c.201T>G	ENSP00000363129.3:p.Ala67=
ENST00000374018.5:c.15T>G	ENSP00000363130.1:p.Ala5=
ENST00000474635.1:n.130T>G
NM_003093.2:c.138T>G	NP_003084.1:p.Ala46=
NR_029472.1:n.545T>G
NM_003093.3:c.138T>G MANE Select	NP_003084.1:p.Ala46=
NR_029472.2:n.134T>G