Canonical Allele Identifier: CA1556800432
Gene: CRHBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968433G= , CM000667.2:g.76968433G= GRCh38
NC_000005.9:g.76264258G= , CM000667.1:g.76264258G= GRCh37
NC_000005.8:g.76300014G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274368.9:c.812-295G= MANE Select ENSP00000274368.4:n.812-295G=
ENST00000274368.8:c.812-295G= ENSP00000274368.4:n.812-295G=
ENST00000503763.1:n.227-295G=
ENST00000514258.1:n.311+4973G=
NM_001882.3:c.812-295G= NP_001873.2:n.812-295G=
XR_948235.1:n.1111+4973G=
XR_948235.3:n.1091+4973G=
NM_001882.4:c.812-295G= MANE Select NP_001873.2:n.812-295G=
Search 100 bp 5'
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