Canonical Allele Identifier: CA1697942210

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30968997C= , CM000669.2:g.30968997C=	GRCh38
NC_000007.13:g.31008612C= , CM000669.1:g.31008612C=	GRCh37
NC_000007.12:g.30975137C=	NCBI36
NG_021416.1:g.9977C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326139.7:c.160+61C= MANE Select	ENSP00000320180.2:n.160+61C=
ENST00000326139.6:c.160+61C=	ENSP00000320180.2:n.160+61C=
NM_000823.3:c.160+61C=	NP_000814.2:n.160+61C=
NM_000823.4:c.160+61C= MANE Select	NP_000814.2:n.160+61C=