Canonical Allele Identifier: CA449892523
Gene: SNRPC HGNC NCBI

Linked Data

gnomAD v4: 6-34762624-A-G
MyVariant Identifiers: chr6:g.34730401A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762624A>G , CM000668.2:g.34762624A>G GRCh38
NC_000006.11:g.34730401A>G , CM000668.1:g.34730401A>G GRCh37
NC_000006.10:g.34838379A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.81A>G MANE Select ENSP00000244520.5:p.Gly27=
ENST00000244520.9:c.81A>G ENSP00000244520.5:p.Gly27=
ENST00000374017.3:c.144A>G ENSP00000363129.3:p.Gly48=
ENST00000374018.5:c.-43A>G ENSP00000363130.1:n.-43A>G
ENST00000474635.1:n.73A>G
NM_003093.2:c.81A>G NP_003084.1:p.Gly27=
NR_029472.1:n.488A>G
NM_003093.3:c.81A>G MANE Select NP_003084.1:p.Gly27=
NR_029472.2:n.77A>G
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