Canonical Allele Identifier: CA1420511889

Gene: GHSR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172448327C= , CM000665.2:g.172448327C=	GRCh38
NC_000003.11:g.172166117C= , CM000665.1:g.172166117C=	GRCh37
NC_000003.10:g.173648811C=	NCBI36
NG_021159.1:g.5130G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.87G= MANE Select	ENSP00000241256.2:p.Ser29=
ENST00000241256.2:c.87G=	ENSP00000241256.2:p.Ser29=
ENST00000427970.1:c.87G=	ENSP00000395344.1:p.Ser29=
NM_004122.2:c.87G=	NP_004113.1:p.Ser29=
NM_198407.2:c.87G= MANE Select	NP_940799.1:p.Ser29=