Canonical Allele Identifier: CA355515148
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448119C>A , CM000665.2:g.172448119C>A GRCh38
NC_000003.11:g.172165909C>A , CM000665.1:g.172165909C>A GRCh37
NC_000003.10:g.173648603C>A NCBI36
NG_021159.1:g.5338G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.295G>T MANE Select ENSP00000241256.2:p.Asp99Tyr
ENST00000241256.2:c.295G>T ENSP00000241256.2:p.Asp99Tyr
ENST00000427970.1:c.295G>T ENSP00000395344.1:p.Asp99Tyr
NM_004122.2:c.295G>T NP_004113.1:p.Asp99Tyr
NM_198407.2:c.295G>T MANE Select NP_940799.1:p.Asp99Tyr