Canonical Allele Identifier: CA355516588
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448304A>G , CM000665.2:g.172448304A>G GRCh38
NC_000003.11:g.172166094A>G , CM000665.1:g.172166094A>G GRCh37
NC_000003.10:g.173648788A>G NCBI36
NG_021159.1:g.5153T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.110T>C MANE Select ENSP00000241256.2:p.Leu37Pro
ENST00000241256.2:c.110T>C ENSP00000241256.2:p.Leu37Pro
ENST00000427970.1:c.110T>C ENSP00000395344.1:p.Leu37Pro
NM_004122.2:c.110T>C NP_004113.1:p.Leu37Pro
NM_198407.2:c.110T>C MANE Select NP_940799.1:p.Leu37Pro