Canonical Allele Identifier: CA1556800398

Gene: CRHBP

Linked Data

• dbSNP Id: rs1745894397

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76968416C>G , CM000667.2:g.76968416C>G	GRCh38
NC_000005.9:g.76264241C>G , CM000667.1:g.76264241C>G	GRCh37
NC_000005.8:g.76299997C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274368.9:c.812-312C>G MANE Select	ENSP00000274368.4:n.812-312C>G
ENST00000274368.8:c.812-312C>G	ENSP00000274368.4:n.812-312C>G
ENST00000503763.1:n.227-312C>G
ENST00000514258.1:n.311+4956C>G
NM_001882.3:c.812-312C>G	NP_001873.2:n.812-312C>G
XR_948235.1:n.1111+4956C>G
XR_948235.3:n.1091+4956C>G
NM_001882.4:c.812-312C>G MANE Select	NP_001873.2:n.812-312C>G