Canonical Allele Identifier: CA449892521
Gene: SNRPC HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.34730398T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762621T>C , CM000668.2:g.34762621T>C GRCh38
NC_000006.11:g.34730398T>C , CM000668.1:g.34730398T>C GRCh37
NC_000006.10:g.34838376T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.78T>C MANE Select ENSP00000244520.5:p.Ser26=
ENST00000244520.9:c.78T>C ENSP00000244520.5:p.Ser26=
ENST00000374017.3:c.141T>C ENSP00000363129.3:p.Ser47=
ENST00000374018.5:c.-46T>C ENSP00000363130.1:n.-46T>C
ENST00000474635.1:n.70T>C
NM_003093.2:c.78T>C NP_003084.1:p.Ser26=
NR_029472.1:n.485T>C
NM_003093.3:c.78T>C MANE Select NP_003084.1:p.Ser26=
NR_029472.2:n.74T>C
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