Canonical Allele Identifier: CA178436209
Gene: CRH HGNC NCBI
dbSNP:
28364015
gnomAD v2:
8:67090899 A / G
gnomAD v3:
8:66178664 A / G
gnomAD v4:
chr8-66178664-A-G
Joint Max Group AF 0.00004765 (NFE)
Genomes Max Group AF 0.00004765 (NFE)
MyVariant.info:
GRCh38 chr8:g.66178664A>G
GRCh37 chr8:g.67090899A>G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66178664A>G , CM000670.2:g.66178664A>G GRCh38
NC_000008.10:g.67090899A>G , CM000670.1:g.67090899A>G GRCh37
NC_000008.9:g.67253453A>G NCBI36
NG_016127.1:g.4800T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000276571.4:c.-386T>C ENSP00000276571.3:n.-386T>C
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