Canonical Allele Identifier: CA87784250
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs185502038
gnomAD v2: 3-172165085-A-G
gnomAD v3: 3-172447295-A-G
gnomAD v4: 3-172447295-A-G
MyVariant Identifiers: chr3:g.172165085A>G (hg19) chr3:g.172447295A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447295A>G , CM000665.2:g.172447295A>G GRCh38
NC_000003.11:g.172165085A>G , CM000665.1:g.172165085A>G GRCh37
NC_000003.10:g.173647779A>G NCBI36
NG_021159.1:g.6162T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.796+323T>C MANE Select ENSP00000241256.2:n.796+323T>C
ENST00000241256.2:c.796+323T>C ENSP00000241256.2:n.796+323T>C
NM_198407.2:c.796+323T>C MANE Select NP_940799.1:n.796+323T>C
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