Canonical Allele Identifier: CA1420511884
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448318G= , CM000665.2:g.172448318G= GRCh38
NC_000003.11:g.172166108G= , CM000665.1:g.172166108G= GRCh37
NC_000003.10:g.173648802G= NCBI36
NG_021159.1:g.5139C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.96C= MANE Select ENSP00000241256.2:p.Asp32=
ENST00000241256.2:c.96C= ENSP00000241256.2:p.Asp32=
ENST00000427970.1:c.96C= ENSP00000395344.1:p.Asp32=
NM_004122.2:c.96C= NP_004113.1:p.Asp32=
NM_198407.2:c.96C= MANE Select NP_940799.1:p.Asp32=