Canonical Allele Identifier: CA1556800560
Gene: CRHBP HGNC NCBI

Linked Data

dbSNP Id: rs1745896351
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968526A>C , CM000667.2:g.76968526A>C GRCh38
NC_000005.9:g.76264351A>C , CM000667.1:g.76264351A>C GRCh37
NC_000005.8:g.76300107A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274368.9:c.812-202A>C MANE Select ENSP00000274368.4:n.812-202A>C
ENST00000274368.8:c.812-202A>C ENSP00000274368.4:n.812-202A>C
ENST00000503763.1:n.227-202A>C
ENST00000514258.1:n.311+5066A>C
NM_001882.3:c.812-202A>C NP_001873.2:n.812-202A>C
XR_948235.1:n.1111+5066A>C
XR_948235.3:n.1091+5066A>C
NM_001882.4:c.812-202A>C MANE Select NP_001873.2:n.812-202A>C
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