Canonical Allele Identifier: CA1420511386
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447382G= , CM000665.2:g.172447382G= GRCh38
NC_000003.11:g.172165172G= , CM000665.1:g.172165172G= GRCh37
NC_000003.10:g.173647866G= NCBI36
NG_021159.1:g.6075C=

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+236C= MANE Select ENSP00000241256.2:n.796+236C=
ENST00000241256.2:c.796+236C= ENSP00000241256.2:n.796+236C=
NM_198407.2:c.796+236C= MANE Select NP_940799.1:n.796+236C=