Canonical Allele Identifier: CA355514521

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165777A>C (hg19) ; chr3:g.172447987A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447987A>C , CM000665.2:g.172447987A>C	GRCh38
NC_000003.11:g.172165777A>C , CM000665.1:g.172165777A>C	GRCh37
NC_000003.10:g.173648471A>C	NCBI36
NG_021159.1:g.5470T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.427T>G MANE Select	ENSP00000241256.2:p.Phe143Val
ENST00000241256.2:c.427T>G	ENSP00000241256.2:p.Phe143Val
ENST00000427970.1:c.427T>G	ENSP00000395344.1:p.Phe143Val
NM_004122.2:c.427T>G	NP_004113.1:p.Phe143Val
NM_198407.2:c.427T>G MANE Select	NP_940799.1:p.Phe143Val