Canonical Allele Identifier: CA1420511329
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447294C= , CM000665.2:g.172447294C= GRCh38
NC_000003.11:g.172165084C= , CM000665.1:g.172165084C= GRCh37
NC_000003.10:g.173647778C= NCBI36
NG_021159.1:g.6163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.796+324G= MANE Select ENSP00000241256.2:n.796+324G=
ENST00000241256.2:c.796+324G= ENSP00000241256.2:n.796+324G=
NM_198407.2:c.796+324G= MANE Select NP_940799.1:n.796+324G=