Canonical Allele Identifier: CA355516181
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448214A>T , CM000665.2:g.172448214A>T GRCh38
NC_000003.11:g.172166004A>T , CM000665.1:g.172166004A>T GRCh37
NC_000003.10:g.173648698A>T NCBI36
NG_021159.1:g.5243T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.200T>A MANE Select ENSP00000241256.2:p.Val67Glu
ENST00000241256.2:c.200T>A ENSP00000241256.2:p.Val67Glu
ENST00000427970.1:c.200T>A ENSP00000395344.1:p.Val67Glu
NM_004122.2:c.200T>A NP_004113.1:p.Val67Glu
NM_198407.2:c.200T>A MANE Select NP_940799.1:p.Val67Glu