Canonical Allele Identifier: CA436965657
Gene: GHSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172166087G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448297G>T , CM000665.2:g.172448297G>T GRCh38
NC_000003.11:g.172166087G>T , CM000665.1:g.172166087G>T GRCh37
NC_000003.10:g.173648781G>T NCBI36
NG_021159.1:g.5160C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.117C>A MANE Select ENSP00000241256.2:p.Pro39=
ENST00000241256.2:c.117C>A ENSP00000241256.2:p.Pro39=
ENST00000427970.1:c.117C>A ENSP00000395344.1:p.Pro39=
NM_004122.2:c.117C>A NP_004113.1:p.Pro39=
NM_198407.2:c.117C>A MANE Select NP_940799.1:p.Pro39=
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