Canonical Allele Identifier: CA1420511330
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447295A= , CM000665.2:g.172447295A= GRCh38
NC_000003.11:g.172165085A= , CM000665.1:g.172165085A= GRCh37
NC_000003.10:g.173647779A= NCBI36
NG_021159.1:g.6162T=

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+323T= MANE Select ENSP00000241256.2:n.796+323T=
ENST00000241256.2:c.796+323T= ENSP00000241256.2:n.796+323T=
NM_198407.2:c.796+323T= MANE Select NP_940799.1:n.796+323T=