Canonical Allele Identifier: CA1420511959
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1737544934
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448452C>G , CM000665.2:g.172448452C>G GRCh38
NC_000003.11:g.172166242C>G , CM000665.1:g.172166242C>G GRCh37
NC_000003.10:g.173648936C>G NCBI36
NG_021159.1:g.5005G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.-39G>C MANE Select ENSP00000241256.2:n.-39G>C
ENST00000241256.2:c.-39G>C ENSP00000241256.2:n.-39G>C
ENST00000427970.1:c.-39G>C ENSP00000395344.1:n.-39G>C
NM_004122.2:c.-39G>C NP_004113.1:n.-39G>C
NM_198407.2:c.-39G>C MANE Select NP_940799.1:n.-39G>C
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