Canonical Allele Identifier: CA1420511380
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs2948694
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447373A>T , CM000665.2:g.172447373A>T GRCh38
NC_000003.11:g.172165163A>T , CM000665.1:g.172165163A>T GRCh37
NC_000003.10:g.173647857A>T NCBI36
NG_021159.1:g.6084T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+245T>A MANE Select ENSP00000241256.2:n.796+245T>A
ENST00000241256.2:c.796+245T>A ENSP00000241256.2:n.796+245T>A
NM_198407.2:c.796+245T>A MANE Select NP_940799.1:n.796+245T>A
Search 100 bp 5'
Search 100 bp 3'