Canonical Allele Identifier: CA2678360481
Gene: SNRPC HGNC NCBI

Linked Data

gnomAD v4: 6-34762535-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762535A>T , CM000668.2:g.34762535A>T GRCh38
NC_000006.11:g.34730312A>T , CM000668.1:g.34730312A>T GRCh37
NC_000006.10:g.34838290A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.52-60A>T MANE Select ENSP00000244520.5:n.52-60A>T
ENST00000244520.9:c.52-60A>T ENSP00000244520.5:n.52-60A>T
ENST00000374017.3:c.115-60A>T ENSP00000363129.3:n.115-60A>T
ENST00000374018.5:c.-72-60A>T ENSP00000363130.1:n.-72-60A>T
ENST00000474635.1:n.44-60A>T
NM_003093.2:c.52-60A>T NP_003084.1:n.52-60A>T
NR_029472.1:n.459-60A>T
NM_003093.3:c.52-60A>T MANE Select NP_003084.1:n.52-60A>T
NR_029472.2:n.48-60A>T