Canonical Allele Identifier: CA355514695
Gene: GHSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172165807T>A (hg19) chr3:g.172448017T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448017T>A , CM000665.2:g.172448017T>A GRCh38
NC_000003.11:g.172165807T>A , CM000665.1:g.172165807T>A GRCh37
NC_000003.10:g.173648501T>A NCBI36
NG_021159.1:g.5440A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.397A>T MANE Select ENSP00000241256.2:p.Thr133Ser
ENST00000241256.2:c.397A>T ENSP00000241256.2:p.Thr133Ser
ENST00000427970.1:c.397A>T ENSP00000395344.1:p.Thr133Ser
NM_004122.2:c.397A>T NP_004113.1:p.Thr133Ser
NM_198407.2:c.397A>T MANE Select NP_940799.1:p.Thr133Ser
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