Canonical Allele Identifier: CA2668560012
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447394_172447399del , CM000665.2:g.172447394_172447399del GRCh38
NC_000003.11:g.172165184_172165189del , CM000665.1:g.172165184_172165189del GRCh37
NC_000003.10:g.173647878_173647883del NCBI36
NG_021159.1:g.6064_6069del

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+225_796+230del MANE Select ENSP00000241256.2:n.796+225_796+230del
ENST00000241256.2:c.796+225_796+230del ENSP00000241256.2:n.796+225_796+230del
NM_198407.2:c.796+225_796+230del MANE Select NP_940799.1:n.796+225_796+230del