Canonical Allele Identifier: CA1420511885

Gene: GHSR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172448320C= , CM000665.2:g.172448320C=	GRCh38
NC_000003.11:g.172166110C= , CM000665.1:g.172166110C=	GRCh37
NC_000003.10:g.173648804C=	NCBI36
NG_021159.1:g.5137G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.94G= MANE Select	ENSP00000241256.2:p.Asp32=
ENST00000241256.2:c.94G=	ENSP00000241256.2:p.Asp32=
ENST00000427970.1:c.94G=	ENSP00000395344.1:p.Asp32=
NM_004122.2:c.94G=	NP_004113.1:p.Asp32=
NM_198407.2:c.94G= MANE Select	NP_940799.1:p.Asp32=