Canonical Allele Identifier: CA917066217
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1553806830

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447389del , CM000665.2:g.172447389del GRCh38
NC_000003.11:g.172165179del , CM000665.1:g.172165179del GRCh37
NC_000003.10:g.173647873del NCBI36
NG_021159.1:g.6068del

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+229del MANE Select ENSP00000241256.2:n.796+229del
ENST00000241256.2:c.796+229del ENSP00000241256.2:n.796+229del
NM_198407.2:c.796+229del MANE Select NP_940799.1:n.796+229del