Canonical Allele Identifier: CA902678951
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1167548037
MyVariant Identifiers: chr3:g.172165101G>C (hg19) chr3:g.172447311G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447311G>C , CM000665.2:g.172447311G>C GRCh38
NC_000003.11:g.172165101G>C , CM000665.1:g.172165101G>C GRCh37
NC_000003.10:g.173647795G>C NCBI36
NG_021159.1:g.6146C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+307C>G MANE Select ENSP00000241256.2:n.796+307C>G
ENST00000241256.2:c.796+307C>G ENSP00000241256.2:n.796+307C>G
NM_198407.2:c.796+307C>G MANE Select NP_940799.1:n.796+307C>G
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