Canonical Allele Identifier: CA1556800444
Gene: CRHBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968436A= , CM000667.2:g.76968436A= GRCh38
NC_000005.9:g.76264261A= , CM000667.1:g.76264261A= GRCh37
NC_000005.8:g.76300017A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274368.9:c.812-292A= MANE Select ENSP00000274368.4:n.812-292A=
ENST00000274368.8:c.812-292A= ENSP00000274368.4:n.812-292A=
ENST00000503763.1:n.227-292A=
ENST00000514258.1:n.311+4976A=
NM_001882.3:c.812-292A= NP_001873.2:n.812-292A=
XR_948235.1:n.1111+4976A=
XR_948235.3:n.1091+4976A=
NM_001882.4:c.812-292A= MANE Select NP_001873.2:n.812-292A=