Canonical Allele Identifier: CA355515068
Gene: GHSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172165888A>T (hg19) chr3:g.172448098A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448098A>T , CM000665.2:g.172448098A>T GRCh38
NC_000003.11:g.172165888A>T , CM000665.1:g.172165888A>T GRCh37
NC_000003.10:g.173648582A>T NCBI36
NG_021159.1:g.5359T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.316T>A MANE Select ENSP00000241256.2:p.Tyr106Asn
ENST00000241256.2:c.316T>A ENSP00000241256.2:p.Tyr106Asn
ENST00000427970.1:c.316T>A ENSP00000395344.1:p.Tyr106Asn
NM_004122.2:c.316T>A NP_004113.1:p.Tyr106Asn
NM_198407.2:c.316T>A MANE Select NP_940799.1:p.Tyr106Asn
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