Canonical Allele Identifier: CA2668560011
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447387_172447388del , CM000665.2:g.172447387_172447388del GRCh38
NC_000003.11:g.172165177_172165178del , CM000665.1:g.172165177_172165178del GRCh37
NC_000003.10:g.173647871_173647872del NCBI36
NG_021159.1:g.6069_6070del

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+230_796+231del MANE Select ENSP00000241256.2:n.796+230_796+231del
ENST00000241256.2:c.796+230_796+231del ENSP00000241256.2:n.796+230_796+231del
NM_198407.2:c.796+230_796+231del MANE Select NP_940799.1:n.796+230_796+231del