Canonical Allele Identifier: CA355514858
Gene: GHSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172165834C>A (hg19) chr3:g.172448044C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448044C>A , CM000665.2:g.172448044C>A GRCh38
NC_000003.11:g.172165834C>A , CM000665.1:g.172165834C>A GRCh37
NC_000003.10:g.173648528C>A NCBI36
NG_021159.1:g.5413G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.370G>T MANE Select ENSP00000241256.2:p.Glu124Ter
ENST00000241256.2:c.370G>T ENSP00000241256.2:p.Glu124Ter
ENST00000427970.1:c.370G>T ENSP00000395344.1:p.Glu124Ter
NM_004122.2:c.370G>T NP_004113.1:p.Glu124Ter
NM_198407.2:c.370G>T MANE Select NP_940799.1:p.Glu124Ter
Search 100 bp 5'
Search 100 bp 3'