Canonical Allele Identifier: CA355514390

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165740A>T (hg19) ; chr3:g.172447950A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447950A>T , CM000665.2:g.172447950A>T	GRCh38
NC_000003.11:g.172165740A>T , CM000665.1:g.172165740A>T	GRCh37
NC_000003.10:g.173648434A>T	NCBI36
NG_021159.1:g.5507T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.464T>A MANE Select	ENSP00000241256.2:p.Val155Asp
ENST00000241256.2:c.464T>A	ENSP00000241256.2:p.Val155Asp
ENST00000427970.1:c.464T>A	ENSP00000395344.1:p.Val155Asp
NM_004122.2:c.464T>A	NP_004113.1:p.Val155Asp
NM_198407.2:c.464T>A MANE Select	NP_940799.1:p.Val155Asp