Canonical Allele Identifier: CA917066215
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs398106748

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447388dup , CM000665.2:g.172447388dup GRCh38
NC_000003.11:g.172165178dup , CM000665.1:g.172165178dup GRCh37
NC_000003.10:g.173647872dup NCBI36
NG_021159.1:g.6070dup

Transcript Alleles

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