Canonical Allele Identifier: CA355516857
Gene: GHSR HGNC NCBI

Linked Data

gnomAD v4: 3-172448371-T-G
MyVariant Identifiers: chr3:g.172166161T>G (hg19) chr3:g.172448371T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448371T>G , CM000665.2:g.172448371T>G GRCh38
NC_000003.11:g.172166161T>G , CM000665.1:g.172166161T>G GRCh37
NC_000003.10:g.173648855T>G NCBI36
NG_021159.1:g.5086A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.43A>C MANE Select ENSP00000241256.2:p.Thr15Pro
ENST00000241256.2:c.43A>C ENSP00000241256.2:p.Thr15Pro
ENST00000427970.1:c.43A>C ENSP00000395344.1:p.Thr15Pro
NM_004122.2:c.43A>C NP_004113.1:p.Thr15Pro
NM_198407.2:c.43A>C MANE Select NP_940799.1:p.Thr15Pro
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