Canonical Allele Identifier: CA355514284

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165689A>T (hg19) ; chr3:g.172447899A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447899A>T , CM000665.2:g.172447899A>T	GRCh38
NC_000003.11:g.172165689A>T , CM000665.1:g.172165689A>T	GRCh37
NC_000003.10:g.173648383A>T	NCBI36
NG_021159.1:g.5558T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.515T>A MANE Select	ENSP00000241256.2:p.Phe172Tyr
ENST00000241256.2:c.515T>A	ENSP00000241256.2:p.Phe172Tyr
ENST00000427970.1:c.515T>A	ENSP00000395344.1:p.Phe172Tyr
NM_004122.2:c.515T>A	NP_004113.1:p.Phe172Tyr
NM_198407.2:c.515T>A MANE Select	NP_940799.1:p.Phe172Tyr