Canonical Allele Identifier: CA1420511788
Gene: GHSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448143G= , CM000665.2:g.172448143G= GRCh38
NC_000003.11:g.172165933G= , CM000665.1:g.172165933G= GRCh37
NC_000003.10:g.173648627G= NCBI36
NG_021159.1:g.5314C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.271C= MANE Select ENSP00000241256.2:p.Leu91=
ENST00000241256.2:c.271C= ENSP00000241256.2:p.Leu91=
ENST00000427970.1:c.271C= ENSP00000395344.1:p.Leu91=
NM_004122.2:c.271C= NP_004113.1:p.Leu91=
NM_198407.2:c.271C= MANE Select NP_940799.1:p.Leu91=