Canonical Allele Identifier: CA1556800641
Gene: CRHBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968596T= , CM000667.2:g.76968596T= GRCh38
NC_000005.9:g.76264421T= , CM000667.1:g.76264421T= GRCh37
NC_000005.8:g.76300177T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274368.9:c.812-132T= MANE Select ENSP00000274368.4:n.812-132T=
ENST00000274368.8:c.812-132T= ENSP00000274368.4:n.812-132T=
ENST00000503763.1:n.227-132T=
ENST00000514258.1:n.311+5136T=
NM_001882.3:c.812-132T= NP_001873.2:n.812-132T=
XR_948235.1:n.1111+5136T=
XR_948235.3:n.1091+5136T=
NM_001882.4:c.812-132T= MANE Select NP_001873.2:n.812-132T=
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