Canonical Allele Identifier: CA1420511699
Gene: GHSR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447952C= , CM000665.2:g.172447952C= GRCh38
NC_000003.11:g.172165742C= , CM000665.1:g.172165742C= GRCh37
NC_000003.10:g.173648436C= NCBI36
NG_021159.1:g.5505G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.462G= MANE Select ENSP00000241256.2:p.Val154=
ENST00000241256.2:c.462G= ENSP00000241256.2:p.Val154=
ENST00000427970.1:c.462G= ENSP00000395344.1:p.Val154=
NM_004122.2:c.462G= NP_004113.1:p.Val154=
NM_198407.2:c.462G= MANE Select NP_940799.1:p.Val154=
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