Canonical Allele Identifier: CA363727955
Gene: SNRPC HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.34730403G>C (hg19) chr6:g.34762626G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762626G>C , CM000668.2:g.34762626G>C GRCh38
NC_000006.11:g.34730403G>C , CM000668.1:g.34730403G>C GRCh37
NC_000006.10:g.34838381G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.83G>C MANE Select ENSP00000244520.5:p.Arg28Thr
ENST00000244520.9:c.83G>C ENSP00000244520.5:p.Arg28Thr
ENST00000374017.3:c.146G>C ENSP00000363129.3:p.Arg49Thr
ENST00000374018.5:c.-41G>C ENSP00000363130.1:n.-41G>C
ENST00000474635.1:n.75G>C
NM_003093.2:c.83G>C NP_003084.1:p.Arg28Thr
NR_029472.1:n.490G>C
NM_003093.3:c.83G>C MANE Select NP_003084.1:p.Arg28Thr
NR_029472.2:n.79G>C
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