Canonical Allele Identifier: CA436965692
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs137953416
gnomAD v2: 3-172166117-C-T
gnomAD v3: 3-172448327-C-T
gnomAD v4: 3-172448327-C-T
MyVariant Identifiers: chr3:g.172166117C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448327C>T , CM000665.2:g.172448327C>T GRCh38
NC_000003.11:g.172166117C>T , CM000665.1:g.172166117C>T GRCh37
NC_000003.10:g.173648811C>T NCBI36
NG_021159.1:g.5130G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.87G>A MANE Select ENSP00000241256.2:p.Ser29=
ENST00000241256.2:c.87G>A ENSP00000241256.2:p.Ser29=
ENST00000427970.1:c.87G>A ENSP00000395344.1:p.Ser29=
NM_004122.2:c.87G>A NP_004113.1:p.Ser29=
NM_198407.2:c.87G>A MANE Select NP_940799.1:p.Ser29=
Search 100 bp 5'
Search 100 bp 3'