Canonical Allele Identifier: CA1420511343
Gene: GHSR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447327G= , CM000665.2:g.172447327G= GRCh38
NC_000003.11:g.172165117G= , CM000665.1:g.172165117G= GRCh37
NC_000003.10:g.173647811G= NCBI36
NG_021159.1:g.6130C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.796+291C= MANE Select ENSP00000241256.2:n.796+291C=
ENST00000241256.2:c.796+291C= ENSP00000241256.2:n.796+291C=
NM_198407.2:c.796+291C= MANE Select NP_940799.1:n.796+291C=
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