Canonical Allele Identifier: CA363728149

Gene: SNRPC

Linked Data

• MyVariant Identifiers: chr6:g.34730478C>T (hg19) ; chr6:g.34762701C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762701C>T , CM000668.2:g.34762701C>T	GRCh38
NC_000006.11:g.34730478C>T , CM000668.1:g.34730478C>T	GRCh37
NC_000006.10:g.34838456C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244520.10:c.158C>T MANE Select	ENSP00000244520.5:p.Thr53Ile
ENST00000244520.9:c.158C>T	ENSP00000244520.5:p.Thr53Ile
ENST00000374017.3:c.221C>T	ENSP00000363129.3:p.Thr74Ile
ENST00000374018.5:c.35C>T	ENSP00000363130.1:p.Thr12Ile
ENST00000474635.1:n.150C>T
NM_003093.2:c.158C>T	NP_003084.1:p.Thr53Ile
NR_029472.1:n.565C>T
NM_003093.3:c.158C>T MANE Select	NP_003084.1:p.Thr53Ile
NR_029472.2:n.154C>T