Canonical Allele Identifier: CA1420511346
Gene: GHSR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447332A= , CM000665.2:g.172447332A= GRCh38
NC_000003.11:g.172165122A= , CM000665.1:g.172165122A= GRCh37
NC_000003.10:g.173647816A= NCBI36
NG_021159.1:g.6125T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.796+286T= MANE Select ENSP00000241256.2:n.796+286T=
ENST00000241256.2:c.796+286T= ENSP00000241256.2:n.796+286T=
NM_198407.2:c.796+286T= MANE Select NP_940799.1:n.796+286T=
Search 100 bp 5'
Search 100 bp 3'