Canonical Allele Identifier: CA363727949
Gene: SNRPC HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.34730400G>A (hg19) chr6:g.34762623G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762623G>A , CM000668.2:g.34762623G>A GRCh38
NC_000006.11:g.34730400G>A , CM000668.1:g.34730400G>A GRCh37
NC_000006.10:g.34838378G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.80G>A MANE Select ENSP00000244520.5:p.Gly27Glu
ENST00000244520.9:c.80G>A ENSP00000244520.5:p.Gly27Glu
ENST00000374017.3:c.143G>A ENSP00000363129.3:p.Gly48Glu
ENST00000374018.5:c.-44G>A ENSP00000363130.1:n.-44G>A
ENST00000474635.1:n.72G>A
NM_003093.2:c.80G>A NP_003084.1:p.Gly27Glu
NR_029472.1:n.487G>A
NM_003093.3:c.80G>A MANE Select NP_003084.1:p.Gly27Glu
NR_029472.2:n.76G>A
Search 100 bp 5'
Search 100 bp 3'