Canonical Allele Identifier: CA355515761
Gene: GHSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172165927A>G (hg19) chr3:g.172448137A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448137A>G , CM000665.2:g.172448137A>G GRCh38
NC_000003.11:g.172165927A>G , CM000665.1:g.172165927A>G GRCh37
NC_000003.10:g.173648621A>G NCBI36
NG_021159.1:g.5320T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.277T>C MANE Select ENSP00000241256.2:p.Phe93Leu
ENST00000241256.2:c.277T>C ENSP00000241256.2:p.Phe93Leu
ENST00000427970.1:c.277T>C ENSP00000395344.1:p.Phe93Leu
NM_004122.2:c.277T>C NP_004113.1:p.Phe93Leu
NM_198407.2:c.277T>C MANE Select NP_940799.1:p.Phe93Leu
Search 100 bp 5'
Search 100 bp 3'