Canonical Allele Identifier: CA2711379711
Gene: SNRPC HGNC NCBI

Linked Data

dbSNP Id: rs2127406168
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762530A>G , CM000668.2:g.34762530A>G GRCh38
NC_000006.11:g.34730307A>G , CM000668.1:g.34730307A>G GRCh37
NC_000006.10:g.34838285A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.52-65A>G MANE Select ENSP00000244520.5:n.52-65A>G
ENST00000244520.9:c.52-65A>G ENSP00000244520.5:n.52-65A>G
ENST00000374017.3:c.115-65A>G ENSP00000363129.3:n.115-65A>G
ENST00000374018.5:c.-72-65A>G ENSP00000363130.1:n.-72-65A>G
ENST00000474635.1:n.44-65A>G
NM_003093.2:c.52-65A>G NP_003084.1:n.52-65A>G
NR_029472.1:n.459-65A>G
NM_003093.3:c.52-65A>G MANE Select NP_003084.1:n.52-65A>G
NR_029472.2:n.48-65A>G
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