Canonical Allele Identifier: CA436965819

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165688G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447898G>A , CM000665.2:g.172447898G>A	GRCh38
NC_000003.11:g.172165688G>A , CM000665.1:g.172165688G>A	GRCh37
NC_000003.10:g.173648382G>A	NCBI36
NG_021159.1:g.5559C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.516C>T MANE Select	ENSP00000241256.2:p.Phe172=
ENST00000241256.2:c.516C>T	ENSP00000241256.2:p.Phe172=
ENST00000427970.1:c.516C>T	ENSP00000395344.1:p.Phe172=
NM_004122.2:c.516C>T	NP_004113.1:p.Phe172=
NM_198407.2:c.516C>T MANE Select	NP_940799.1:p.Phe172=