Canonical Allele Identifier: CA363727969
Gene: SNRPC HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.34730408C>T (hg19) chr6:g.34762631C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762631C>T , CM000668.2:g.34762631C>T GRCh38
NC_000006.11:g.34730408C>T , CM000668.1:g.34730408C>T GRCh37
NC_000006.10:g.34838386C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.88C>T MANE Select ENSP00000244520.5:p.His30Tyr
ENST00000244520.9:c.88C>T ENSP00000244520.5:p.His30Tyr
ENST00000374017.3:c.151C>T ENSP00000363129.3:p.His51Tyr
ENST00000374018.5:c.-36C>T ENSP00000363130.1:n.-36C>T
ENST00000474635.1:n.80C>T
NM_003093.2:c.88C>T NP_003084.1:p.His30Tyr
NR_029472.1:n.495C>T
NM_003093.3:c.88C>T MANE Select NP_003084.1:p.His30Tyr
NR_029472.2:n.84C>T
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