Canonical Allele Identifier: CA1420511903
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448354G= , CM000665.2:g.172448354G= GRCh38
NC_000003.11:g.172166144G= , CM000665.1:g.172166144G= GRCh37
NC_000003.10:g.173648838G= NCBI36
NG_021159.1:g.5103C=

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.60C= MANE Select ENSP00000241256.2:p.Asp20=
ENST00000241256.2:c.60C= ENSP00000241256.2:p.Asp20=
ENST00000427970.1:c.60C= ENSP00000395344.1:p.Asp20=
NM_004122.2:c.60C= NP_004113.1:p.Asp20=
NM_198407.2:c.60C= MANE Select NP_940799.1:p.Asp20=