Canonical Allele Identifier: CA436966076

Gene: GHSR

Linked Data

• MyVariant Identifiers: chr3:g.172165760T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172447970T>C , CM000665.2:g.172447970T>C	GRCh38
NC_000003.11:g.172165760T>C , CM000665.1:g.172165760T>C	GRCh37
NC_000003.10:g.173648454T>C	NCBI36
NG_021159.1:g.5487A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241256.3:c.444A>G MANE Select	ENSP00000241256.2:p.Pro148=
ENST00000241256.2:c.444A>G	ENSP00000241256.2:p.Pro148=
ENST00000427970.1:c.444A>G	ENSP00000395344.1:p.Pro148=
NM_004122.2:c.444A>G	NP_004113.1:p.Pro148=
NM_198407.2:c.444A>G MANE Select	NP_940799.1:p.Pro148=