Canonical Allele Identifier: CA1420511696
Gene: GHSR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447946G= , CM000665.2:g.172447946G= GRCh38
NC_000003.11:g.172165736G= , CM000665.1:g.172165736G= GRCh37
NC_000003.10:g.173648430G= NCBI36
NG_021159.1:g.5511C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.468C= MANE Select ENSP00000241256.2:p.Thr156=
ENST00000241256.2:c.468C= ENSP00000241256.2:p.Thr156=
ENST00000427970.1:c.468C= ENSP00000395344.1:p.Thr156=
NM_004122.2:c.468C= NP_004113.1:p.Thr156=
NM_198407.2:c.468C= MANE Select NP_940799.1:p.Thr156=
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