Canonical Allele Identifier: CA355514329

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165710A>T (hg19) ; chr3:g.172447920A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447920A>T , CM000665.2:g.172447920A>T	GRCh38
NC_000003.11:g.172165710A>T , CM000665.1:g.172165710A>T	GRCh37
NC_000003.10:g.173648404A>T	NCBI36
NG_021159.1:g.5537T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.494T>A MANE Select	ENSP00000241256.2:p.Phe165Tyr
ENST00000241256.2:c.494T>A	ENSP00000241256.2:p.Phe165Tyr
ENST00000427970.1:c.494T>A	ENSP00000395344.1:p.Phe165Tyr
NM_004122.2:c.494T>A	NP_004113.1:p.Phe165Tyr
NM_198407.2:c.494T>A MANE Select	NP_940799.1:p.Phe165Tyr