Canonical Allele Identifier: CA87785876
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs963350574
gnomAD v2: 3-172165885-G-A
COSMIC: COSM1238980 COSM1238981
MyVariant Identifiers: chr3:g.172165885G>A (hg19) chr3:g.172448095G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448095G>A , CM000665.2:g.172448095G>A GRCh38
NC_000003.11:g.172165885G>A , CM000665.1:g.172165885G>A GRCh37
NC_000003.10:g.173648579G>A NCBI36
NG_021159.1:g.5362C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.319C>T MANE Select ENSP00000241256.2:p.Arg107Trp
ENST00000241256.2:c.319C>T ENSP00000241256.2:p.Arg107Trp
ENST00000427970.1:c.319C>T ENSP00000395344.1:p.Arg107Trp
NM_004122.2:c.319C>T NP_004113.1:p.Arg107Trp
NM_198407.2:c.319C>T MANE Select NP_940799.1:p.Arg107Trp
Search 100 bp 5'
Search 100 bp 3'