Canonical Allele Identifier: CA1556800439
Gene: CRHBP HGNC NCBI

Linked Data

dbSNP Id: rs1745894976

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968435A>G , CM000667.2:g.76968435A>G GRCh38
NC_000005.9:g.76264260A>G , CM000667.1:g.76264260A>G GRCh37
NC_000005.8:g.76300016A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274368.9:c.812-293A>G MANE Select ENSP00000274368.4:n.812-293A>G
ENST00000274368.8:c.812-293A>G ENSP00000274368.4:n.812-293A>G
ENST00000503763.1:n.227-293A>G
ENST00000514258.1:n.311+4975A>G
NM_001882.3:c.812-293A>G NP_001873.2:n.812-293A>G
XR_948235.1:n.1111+4975A>G
XR_948235.3:n.1091+4975A>G
NM_001882.4:c.812-293A>G MANE Select NP_001873.2:n.812-293A>G