Canonical Allele Identifier: CA436966203
Gene: GHSR HGNC NCBI

Linked Data

COSMIC: COSM5350931 COSM5350932
MyVariant Identifiers: chr3:g.172165793C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448003C>T , CM000665.2:g.172448003C>T GRCh38
NC_000003.11:g.172165793C>T , CM000665.1:g.172165793C>T GRCh37
NC_000003.10:g.173648487C>T NCBI36
NG_021159.1:g.5454G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.411G>A MANE Select ENSP00000241256.2:p.Leu137=
ENST00000241256.2:c.411G>A ENSP00000241256.2:p.Leu137=
ENST00000427970.1:c.411G>A ENSP00000395344.1:p.Leu137=
NM_004122.2:c.411G>A NP_004113.1:p.Leu137=
NM_198407.2:c.411G>A MANE Select NP_940799.1:p.Leu137=
Search 100 bp 5'
Search 100 bp 3'