Canonical Allele Identifier: CA87784267
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs955777725
gnomAD v2: 3-172165117-G-C
gnomAD v3: 3-172447327-G-C
gnomAD v4: 3-172447327-G-C
MyVariant Identifiers: chr3:g.172165117G>C (hg19) chr3:g.172447327G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447327G>C , CM000665.2:g.172447327G>C GRCh38
NC_000003.11:g.172165117G>C , CM000665.1:g.172165117G>C GRCh37
NC_000003.10:g.173647811G>C NCBI36
NG_021159.1:g.6130C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.796+291C>G MANE Select ENSP00000241256.2:n.796+291C>G
ENST00000241256.2:c.796+291C>G ENSP00000241256.2:n.796+291C>G
NM_198407.2:c.796+291C>G MANE Select NP_940799.1:n.796+291C>G
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