Canonical Allele Identifier: CA2599687077
Gene: CRH HGNC NCBI

Linked Data

dbSNP Id: rs2128989126
gnomAD v3: 8-66178688-G-A
gnomAD v4: 8-66178688-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66178688G>A , CM000670.2:g.66178688G>A GRCh38
NC_000008.10:g.67090923G>A , CM000670.1:g.67090923G>A GRCh37
NC_000008.9:g.67253477G>A NCBI36
NG_016127.1:g.4776C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000276571.4:c.-410C>T ENSP00000276571.3:n.-410C>T
Search 100 bp 5'
Search 100 bp 3'