Canonical Allele Identifier: CA363727948
Gene: SNRPC HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.34730399G>A (hg19) chr6:g.34762622G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762622G>A , CM000668.2:g.34762622G>A GRCh38
NC_000006.11:g.34730399G>A , CM000668.1:g.34730399G>A GRCh37
NC_000006.10:g.34838377G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.79G>A MANE Select ENSP00000244520.5:p.Gly27Arg
ENST00000244520.9:c.79G>A ENSP00000244520.5:p.Gly27Arg
ENST00000374017.3:c.142G>A ENSP00000363129.3:p.Gly48Arg
ENST00000374018.5:c.-45G>A ENSP00000363130.1:n.-45G>A
ENST00000474635.1:n.71G>A
NM_003093.2:c.79G>A NP_003084.1:p.Gly27Arg
NR_029472.1:n.486G>A
NM_003093.3:c.79G>A MANE Select NP_003084.1:p.Gly27Arg
NR_029472.2:n.75G>A
Search 100 bp 5'
Search 100 bp 3'