Canonical Allele Identifier: CA1790382990
Gene: CRH HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000276571.4:c.-386T= ENSP00000276571.3:n.-386T=