Canonical Allele Identifier: CA2578860307
Gene: GHRHR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30968983T>A , CM000669.2:g.30968983T>A GRCh38
NC_000007.13:g.31008598T>A , CM000669.1:g.31008598T>A GRCh37
NC_000007.12:g.30975123T>A NCBI36
NG_021416.1:g.9963T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000326139.7:c.160+47T>A MANE Select ENSP00000320180.2:n.160+47T>A
ENST00000326139.6:c.160+47T>A ENSP00000320180.2:n.160+47T>A
NM_000823.3:c.160+47T>A NP_000814.2:n.160+47T>A
NM_000823.4:c.160+47T>A MANE Select NP_000814.2:n.160+47T>A
Search 100 bp 5'
Search 100 bp 3'