Canonical Allele Identifier: CA1420511681
Gene: GHSR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447912A= , CM000665.2:g.172447912A= GRCh38
NC_000003.11:g.172165702A= , CM000665.1:g.172165702A= GRCh37
NC_000003.10:g.173648396A= NCBI36
NG_021159.1:g.5545T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.502T= MANE Select ENSP00000241256.2:p.Trp168=
ENST00000241256.2:c.502T= ENSP00000241256.2:p.Trp168=
ENST00000427970.1:c.502T= ENSP00000395344.1:p.Trp168=
NM_004122.2:c.502T= NP_004113.1:p.Trp168=
NM_198407.2:c.502T= MANE Select NP_940799.1:p.Trp168=
Search 100 bp 5'
Search 100 bp 3'