Canonical Allele Identifier: CA355515859
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448155A>C , CM000665.2:g.172448155A>C GRCh38
NC_000003.11:g.172165945A>C , CM000665.1:g.172165945A>C GRCh37
NC_000003.10:g.173648639A>C NCBI36
NG_021159.1:g.5302T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.259T>G MANE Select ENSP00000241256.2:p.Phe87Val
ENST00000241256.2:c.259T>G ENSP00000241256.2:p.Phe87Val
ENST00000427970.1:c.259T>G ENSP00000395344.1:p.Phe87Val
NM_004122.2:c.259T>G NP_004113.1:p.Phe87Val
NM_198407.2:c.259T>G MANE Select NP_940799.1:p.Phe87Val