Canonical Allele Identifier: CA2668560009
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447386A>C , CM000665.2:g.172447386A>C GRCh38
NC_000003.11:g.172165176A>C , CM000665.1:g.172165176A>C GRCh37
NC_000003.10:g.173647870A>C NCBI36
NG_021159.1:g.6071T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+232T>G MANE Select ENSP00000241256.2:n.796+232T>G
ENST00000241256.2:c.796+232T>G ENSP00000241256.2:n.796+232T>G
NM_198407.2:c.796+232T>G MANE Select NP_940799.1:n.796+232T>G