Canonical Allele Identifier: CA363727943
Gene: SNRPC HGNC NCBI

Linked Data

COSMIC: COSM6174245 COSM6174246
MyVariant Identifiers: chr6:g.34730397G>T (hg19) chr6:g.34762620G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762620G>T , CM000668.2:g.34762620G>T GRCh38
NC_000006.11:g.34730397G>T , CM000668.1:g.34730397G>T GRCh37
NC_000006.10:g.34838375G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.77G>T MANE Select ENSP00000244520.5:p.Ser26Ile
ENST00000244520.9:c.77G>T ENSP00000244520.5:p.Ser26Ile
ENST00000374017.3:c.140G>T ENSP00000363129.3:p.Ser47Ile
ENST00000374018.5:c.-47G>T ENSP00000363130.1:n.-47G>T
ENST00000474635.1:n.69G>T
NM_003093.2:c.77G>T NP_003084.1:p.Ser26Ile
NR_029472.1:n.484G>T
NM_003093.3:c.77G>T MANE Select NP_003084.1:p.Ser26Ile
NR_029472.2:n.73G>T
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Search 100 bp 3'