Canonical Allele Identifier: CA355516711
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448322C>T , CM000665.2:g.172448322C>T GRCh38
NC_000003.11:g.172166112C>T , CM000665.1:g.172166112C>T GRCh37
NC_000003.10:g.173648806C>T NCBI36
NG_021159.1:g.5135G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.92G>A MANE Select ENSP00000241256.2:p.Gly31Asp
ENST00000241256.2:c.92G>A ENSP00000241256.2:p.Gly31Asp
ENST00000427970.1:c.92G>A ENSP00000395344.1:p.Gly31Asp
NM_004122.2:c.92G>A NP_004113.1:p.Gly31Asp
NM_198407.2:c.92G>A MANE Select NP_940799.1:p.Gly31Asp