Canonical Allele Identifier: CA1790382980
Community Standard Title: NC_000008.11:g.66178643C=
Gene: CRH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.66178643C= , CM000670.2:g.66178643C= GRCh38
NC_000008.10:g.67090878C= , CM000670.1:g.67090878C= GRCh37
NC_000008.9:g.67253432C= NCBI36
NG_016127.1:g.4821G=

Transcript Alleles

HGVS Amino-acid Change
NM_000756.3:c.-365G= NP_000747.1:n.-365G=
ENST00000276571.4:c.-365G= ENSP00000276571.3:n.-365G=