Canonical Allele Identifier: CA2668560014
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447388G>A , CM000665.2:g.172447388G>A GRCh38
NC_000003.11:g.172165178G>A , CM000665.1:g.172165178G>A GRCh37
NC_000003.10:g.173647872G>A NCBI36
NG_021159.1:g.6069C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+230C>T MANE Select ENSP00000241256.2:n.796+230C>T
ENST00000241256.2:c.796+230C>T ENSP00000241256.2:n.796+230C>T
NM_198407.2:c.796+230C>T MANE Select NP_940799.1:n.796+230C>T