Canonical Allele Identifier: CA137187045
Gene: SNRPC HGNC NCBI

Linked Data

dbSNP Id: rs935843723
gnomAD v4: 6-34762519-A-C
MyVariant Identifiers: chr6:g.34730296A>C (hg19) chr6:g.34762519A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762519A>C , CM000668.2:g.34762519A>C GRCh38
NC_000006.11:g.34730296A>C , CM000668.1:g.34730296A>C GRCh37
NC_000006.10:g.34838274A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.52-76A>C MANE Select ENSP00000244520.5:n.52-76A>C
ENST00000244520.9:c.52-76A>C ENSP00000244520.5:n.52-76A>C
ENST00000374017.3:c.115-76A>C ENSP00000363129.3:n.115-76A>C
ENST00000374018.5:c.-72-76A>C ENSP00000363130.1:n.-72-76A>C
ENST00000474635.1:n.44-76A>C
NM_003093.2:c.52-76A>C NP_003084.1:n.52-76A>C
NR_029472.1:n.459-76A>C
NM_003093.3:c.52-76A>C MANE Select NP_003084.1:n.52-76A>C
NR_029472.2:n.48-76A>C
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