Canonical Allele Identifier: CA121059186
Gene: CRHBP HGNC NCBI

Linked Data

dbSNP Id: rs968946515
MyVariant Identifiers: chr5:g.76264204G>C (hg19) chr5:g.76968379G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968379G>C , CM000667.2:g.76968379G>C GRCh38
NC_000005.9:g.76264204G>C , CM000667.1:g.76264204G>C GRCh37
NC_000005.8:g.76299960G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274368.9:c.812-349G>C MANE Select ENSP00000274368.4:n.812-349G>C
ENST00000274368.8:c.812-349G>C ENSP00000274368.4:n.812-349G>C
ENST00000503763.1:n.227-349G>C
ENST00000514258.1:n.311+4919G>C
NM_001882.3:c.812-349G>C NP_001873.2:n.812-349G>C
XR_948235.1:n.1111+4919G>C
XR_948235.3:n.1091+4919G>C
NM_001882.4:c.812-349G>C MANE Select NP_001873.2:n.812-349G>C
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