Canonical Allele Identifier: CA355516744
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1247229378

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448338C>G , CM000665.2:g.172448338C>G GRCh38
NC_000003.11:g.172166128C>G , CM000665.1:g.172166128C>G GRCh37
NC_000003.10:g.173648822C>G NCBI36
NG_021159.1:g.5119G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.76G>C MANE Select ENSP00000241256.2:p.Gly26Arg
ENST00000241256.2:c.76G>C ENSP00000241256.2:p.Gly26Arg
ENST00000427970.1:c.76G>C ENSP00000395344.1:p.Gly26Arg
NM_004122.2:c.76G>C NP_004113.1:p.Gly26Arg
NM_198407.2:c.76G>C MANE Select NP_940799.1:p.Gly26Arg