Canonical Allele Identifier: CA355514635
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1737520886
MyVariant Identifiers: chr3:g.172165794A>G (hg19) chr3:g.172448004A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448004A>G , CM000665.2:g.172448004A>G GRCh38
NC_000003.11:g.172165794A>G , CM000665.1:g.172165794A>G GRCh37
NC_000003.10:g.173648488A>G NCBI36
NG_021159.1:g.5453T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.410T>C MANE Select ENSP00000241256.2:p.Leu137Pro
ENST00000241256.2:c.410T>C ENSP00000241256.2:p.Leu137Pro
ENST00000427970.1:c.410T>C ENSP00000395344.1:p.Leu137Pro
NM_004122.2:c.410T>C NP_004113.1:p.Leu137Pro
NM_198407.2:c.410T>C MANE Select NP_940799.1:p.Leu137Pro
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