Canonical Allele Identifier: CA1420511387
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447384G= , CM000665.2:g.172447384G= GRCh38
NC_000003.11:g.172165174G= , CM000665.1:g.172165174G= GRCh37
NC_000003.10:g.173647868G= NCBI36
NG_021159.1:g.6073C=

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+234C= MANE Select ENSP00000241256.2:n.796+234C=
ENST00000241256.2:c.796+234C= ENSP00000241256.2:n.796+234C=
NM_198407.2:c.796+234C= MANE Select NP_940799.1:n.796+234C=