Canonical Allele Identifier: CA363727968
Gene: SNRPC HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.34730408C>G (hg19) chr6:g.34762631C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762631C>G , CM000668.2:g.34762631C>G GRCh38
NC_000006.11:g.34730408C>G , CM000668.1:g.34730408C>G GRCh37
NC_000006.10:g.34838386C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.88C>G MANE Select ENSP00000244520.5:p.His30Asp
ENST00000244520.9:c.88C>G ENSP00000244520.5:p.His30Asp
ENST00000374017.3:c.151C>G ENSP00000363129.3:p.His51Asp
ENST00000374018.5:c.-36C>G ENSP00000363130.1:n.-36C>G
ENST00000474635.1:n.80C>G
NM_003093.2:c.88C>G NP_003084.1:p.His30Asp
NR_029472.1:n.495C>G
NM_003093.3:c.88C>G MANE Select NP_003084.1:p.His30Asp
NR_029472.2:n.84C>G
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