Canonical Allele Identifier: CA363727946
Gene: SNRPC HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.34730399G>C (hg19) chr6:g.34762622G>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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