Canonical Allele Identifier: CA436966032

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165748C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447958C>T , CM000665.2:g.172447958C>T	GRCh38
NC_000003.11:g.172165748C>T , CM000665.1:g.172165748C>T	GRCh37
NC_000003.10:g.173648442C>T	NCBI36
NG_021159.1:g.5499G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.456G>A MANE Select	ENSP00000241256.2:p.Lys152=
ENST00000241256.2:c.456G>A	ENSP00000241256.2:p.Lys152=
ENST00000427970.1:c.456G>A	ENSP00000395344.1:p.Lys152=
NM_004122.2:c.456G>A	NP_004113.1:p.Lys152=
NM_198407.2:c.456G>A MANE Select	NP_940799.1:p.Lys152=