Canonical Allele Identifier: CA2391346968
Gene: CSTB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43776178C= , CM000683.2:g.43776178C= GRCh38
NC_000021.8:g.45196059C= , CM000683.1:g.45196059C= GRCh37
NC_000021.7:g.44020487C= NCBI36
NG_011545.1:g.5201G= , LRG_485:g.5201G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000291568.7:c.66+26G= MANE Select ENSP00000291568.6:n.66+26G=
ENST00000480147.3:n.91G=
ENST00000639959.1:c.35+26G=
ENST00000640406.1:c.66+26G= ENSP00000492672.1:n.66+26G=
ENST00000675996.1:n.153G=
ENST00000291568.5:c.66+26G= ENSP00000291568.5:n.66+26G=
ENST00000480147.1:n.103+26G=
NM_000100.3:c.66+26G= , LRG_485t1:c.66+26G= NP_000091.1:n.66+26G=
NM_000100.4:c.66+26G= MANE Select NP_000091.1:n.66+26G=
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