Canonical Allele Identifier: CA1556800447
Gene: CRHBP HGNC NCBI

Linked Data

dbSNP Id: rs1745895126

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968437A>T , CM000667.2:g.76968437A>T GRCh38
NC_000005.9:g.76264262A>T , CM000667.1:g.76264262A>T GRCh37
NC_000005.8:g.76300018A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274368.9:c.812-291A>T MANE Select ENSP00000274368.4:n.812-291A>T
ENST00000274368.8:c.812-291A>T ENSP00000274368.4:n.812-291A>T
ENST00000503763.1:n.227-291A>T
ENST00000514258.1:n.311+4977A>T
NM_001882.3:c.812-291A>T NP_001873.2:n.812-291A>T
XR_948235.1:n.1111+4977A>T
XR_948235.3:n.1091+4977A>T
NM_001882.4:c.812-291A>T MANE Select NP_001873.2:n.812-291A>T