Canonical Allele Identifier: CA1420511800
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448175A= , CM000665.2:g.172448175A= GRCh38
NC_000003.11:g.172165965A= , CM000665.1:g.172165965A= GRCh37
NC_000003.10:g.173648659A= NCBI36
NG_021159.1:g.5282T=

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.239T= MANE Select ENSP00000241256.2:p.Leu80=
ENST00000241256.2:c.239T= ENSP00000241256.2:p.Leu80=
ENST00000427970.1:c.239T= ENSP00000395344.1:p.Leu80=
NM_004122.2:c.239T= NP_004113.1:p.Leu80=
NM_198407.2:c.239T= MANE Select NP_940799.1:p.Leu80=