Canonical Allele Identifier: CA2578860308

Gene: GHRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30968986T>C , CM000669.2:g.30968986T>C	GRCh38
NC_000007.13:g.31008601T>C , CM000669.1:g.31008601T>C	GRCh37
NC_000007.12:g.30975126T>C	NCBI36
NG_021416.1:g.9966T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326139.7:c.160+50T>C MANE Select	ENSP00000320180.2:n.160+50T>C
ENST00000326139.6:c.160+50T>C	ENSP00000320180.2:n.160+50T>C
NM_000823.3:c.160+50T>C	NP_000814.2:n.160+50T>C
NM_000823.4:c.160+50T>C MANE Select	NP_000814.2:n.160+50T>C