Canonical Allele Identifier: CA121059236
Gene: CRHBP HGNC NCBI

Linked Data

dbSNP Id: rs937015353
MyVariant Identifiers: chr5:g.76264261A>G (hg19) chr5:g.76968436A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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