Canonical Allele Identifier: CA355515749
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448135G>T , CM000665.2:g.172448135G>T GRCh38
NC_000003.11:g.172165925G>T , CM000665.1:g.172165925G>T GRCh37
NC_000003.10:g.173648619G>T NCBI36
NG_021159.1:g.5322C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.279C>A MANE Select ENSP00000241256.2:p.Phe93Leu
ENST00000241256.2:c.279C>A ENSP00000241256.2:p.Phe93Leu
ENST00000427970.1:c.279C>A ENSP00000395344.1:p.Phe93Leu
NM_004122.2:c.279C>A NP_004113.1:p.Phe93Leu
NM_198407.2:c.279C>A MANE Select NP_940799.1:p.Phe93Leu