Canonical Allele Identifier: CA2578590313
Gene: SNRPC HGNC NCBI

Linked Data

gnomAD v4: 6-34762546-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34762546A>T , CM000668.2:g.34762546A>T GRCh38
NC_000006.11:g.34730323A>T , CM000668.1:g.34730323A>T GRCh37
NC_000006.10:g.34838301A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244520.10:c.52-49A>T MANE Select ENSP00000244520.5:n.52-49A>T
ENST00000244520.9:c.52-49A>T ENSP00000244520.5:n.52-49A>T
ENST00000374017.3:c.115-49A>T ENSP00000363129.3:n.115-49A>T
ENST00000374018.5:c.-72-49A>T ENSP00000363130.1:n.-72-49A>T
ENST00000474635.1:n.44-49A>T
NM_003093.2:c.52-49A>T NP_003084.1:n.52-49A>T
NR_029472.1:n.459-49A>T
NM_003093.3:c.52-49A>T MANE Select NP_003084.1:n.52-49A>T
NR_029472.2:n.48-49A>T