Canonical Allele Identifier: CA814093224
Gene: CRHBP HGNC NCBI

Linked Data

dbSNP Id: rs1334219076
MyVariant Identifiers: chr5:g.76264320T>G (hg19) chr5:g.76968495T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968495T>G , CM000667.2:g.76968495T>G GRCh38
NC_000005.9:g.76264320T>G , CM000667.1:g.76264320T>G GRCh37
NC_000005.8:g.76300076T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274368.9:c.812-233T>G MANE Select ENSP00000274368.4:n.812-233T>G
ENST00000274368.8:c.812-233T>G ENSP00000274368.4:n.812-233T>G
ENST00000503763.1:n.227-233T>G
ENST00000514258.1:n.311+5035T>G
NM_001882.3:c.812-233T>G NP_001873.2:n.812-233T>G
XR_948235.1:n.1111+5035T>G
XR_948235.3:n.1091+5035T>G
NM_001882.4:c.812-233T>G MANE Select NP_001873.2:n.812-233T>G
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