Canonical Allele Identifier: CA363727942
Gene: SNRPC HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.34730397G>C (hg19) chr6:g.34762620G>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.77G>C MANE Select ENSP00000244520.5:p.Ser26Thr
ENST00000244520.9:c.77G>C ENSP00000244520.5:p.Ser26Thr
ENST00000374017.3:c.140G>C ENSP00000363129.3:p.Ser47Thr
ENST00000374018.5:c.-47G>C ENSP00000363130.1:n.-47G>C
ENST00000474635.1:n.69G>C
NM_003093.2:c.77G>C NP_003084.1:p.Ser26Thr
NR_029472.1:n.484G>C
NM_003093.3:c.77G>C MANE Select NP_003084.1:p.Ser26Thr
NR_029472.2:n.73G>C
Search 100 bp 5'
Search 100 bp 3'