Canonical Allele Identifier: CA1420511388
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1737488024

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447384G>C , CM000665.2:g.172447384G>C GRCh38
NC_000003.11:g.172165174G>C , CM000665.1:g.172165174G>C GRCh37
NC_000003.10:g.173647868G>C NCBI36
NG_021159.1:g.6073C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+234C>G MANE Select ENSP00000241256.2:n.796+234C>G
ENST00000241256.2:c.796+234C>G ENSP00000241256.2:n.796+234C>G
NM_198407.2:c.796+234C>G MANE Select NP_940799.1:n.796+234C>G