Canonical Allele Identifier: CA2841002663

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30969015A>G , CM000669.2:g.30969015A>G	GRCh38
NC_000007.13:g.31008630A>G , CM000669.1:g.31008630A>G	GRCh37
NC_000007.12:g.30975155A>G	NCBI36
NG_021416.1:g.9995A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326139.7:c.161-48A>G MANE Select	ENSP00000320180.2:n.161-48A>G
ENST00000326139.6:c.161-48A>G	ENSP00000320180.2:n.161-48A>G
NM_000823.3:c.161-48A>G	NP_000814.2:n.161-48A>G
NM_000823.4:c.161-48A>G MANE Select	NP_000814.2:n.161-48A>G