Canonical Allele Identifier: CA1420511874
Gene: GHSR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448301A= , CM000665.2:g.172448301A= GRCh38
NC_000003.11:g.172166091A= , CM000665.1:g.172166091A= GRCh37
NC_000003.10:g.173648785A= NCBI36
NG_021159.1:g.5156T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.113T= MANE Select ENSP00000241256.2:p.Phe38=
ENST00000241256.2:c.113T= ENSP00000241256.2:p.Phe38=
ENST00000427970.1:c.113T= ENSP00000395344.1:p.Phe38=
NM_004122.2:c.113T= NP_004113.1:p.Phe38=
NM_198407.2:c.113T= MANE Select NP_940799.1:p.Phe38=
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