Canonical Allele Identifier: CA355514569

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165784C>A (hg19) ; chr3:g.172447994C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447994C>A , CM000665.2:g.172447994C>A	GRCh38
NC_000003.11:g.172165784C>A , CM000665.1:g.172165784C>A	GRCh37
NC_000003.10:g.173648478C>A	NCBI36
NG_021159.1:g.5463G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.420G>T MANE Select	ENSP00000241256.2:p.Glu140Asp
ENST00000241256.2:c.420G>T	ENSP00000241256.2:p.Glu140Asp
ENST00000427970.1:c.420G>T	ENSP00000395344.1:p.Glu140Asp
NM_004122.2:c.420G>T	NP_004113.1:p.Glu140Asp
NM_198407.2:c.420G>T MANE Select	NP_940799.1:p.Glu140Asp