Canonical Allele Identifier: CA363727973
Gene: SNRPC HGNC NCBI

Linked Data

gnomAD v4: 6-34762633-C-A
MyVariant Identifiers: chr6:g.34730410C>A (hg19) chr6:g.34762633C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762633C>A , CM000668.2:g.34762633C>A GRCh38
NC_000006.11:g.34730410C>A , CM000668.1:g.34730410C>A GRCh37
NC_000006.10:g.34838388C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.90C>A MANE Select ENSP00000244520.5:p.His30Gln
ENST00000244520.9:c.90C>A ENSP00000244520.5:p.His30Gln
ENST00000374017.3:c.153C>A ENSP00000363129.3:p.His51Gln
ENST00000374018.5:c.-34C>A ENSP00000363130.1:n.-34C>A
ENST00000474635.1:n.82C>A
NM_003093.2:c.90C>A NP_003084.1:p.His30Gln
NR_029472.1:n.497C>A
NM_003093.3:c.90C>A MANE Select NP_003084.1:p.His30Gln
NR_029472.2:n.86C>A
Search 100 bp 5'
Search 100 bp 3'