Canonical Allele Identifier: CA1556800668
Gene: CRHBP HGNC NCBI

Linked Data

dbSNP Id: rs1745897720

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968620A>C , CM000667.2:g.76968620A>C GRCh38
NC_000005.9:g.76264445A>C , CM000667.1:g.76264445A>C GRCh37
NC_000005.8:g.76300201A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274368.9:c.812-108A>C MANE Select ENSP00000274368.4:n.812-108A>C
ENST00000274368.8:c.812-108A>C ENSP00000274368.4:n.812-108A>C
ENST00000503763.1:n.227-108A>C
ENST00000514258.1:n.311+5160A>C
NM_001882.3:c.812-108A>C NP_001873.2:n.812-108A>C
XR_948235.1:n.1111+5160A>C
XR_948235.3:n.1091+5160A>C
NM_001882.4:c.812-108A>C MANE Select NP_001873.2:n.812-108A>C