Canonical Allele Identifier: CA355514872
Gene: GHSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172165836C>G (hg19) chr3:g.172448046C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448046C>G , CM000665.2:g.172448046C>G GRCh38
NC_000003.11:g.172165836C>G , CM000665.1:g.172165836C>G GRCh37
NC_000003.10:g.173648530C>G NCBI36
NG_021159.1:g.5411G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.368G>C MANE Select ENSP00000241256.2:p.Ser123Thr
ENST00000241256.2:c.368G>C ENSP00000241256.2:p.Ser123Thr
ENST00000427970.1:c.368G>C ENSP00000395344.1:p.Ser123Thr
NM_004122.2:c.368G>C NP_004113.1:p.Ser123Thr
NM_198407.2:c.368G>C MANE Select NP_940799.1:p.Ser123Thr
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