Canonical Allele Identifier: CA2668559985
Gene: GHSR HGNC NCBI

Linked Data

gnomAD v4: 3-172447358-AAGAAAGACACTGACAAAGTAAAGGGGGAGGAGAGAGAGAGACAGAGACAGAG-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447366_172447417del , CM000665.2:g.172447366_172447417del GRCh38
NC_000003.11:g.172165156_172165207del , CM000665.1:g.172165156_172165207del GRCh37
NC_000003.10:g.173647850_173647901del NCBI36
NG_021159.1:g.6047_6098del

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+208_796+259del MANE Select ENSP00000241256.2:n.796+208_796+259del
ENST00000241256.2:c.796+208_796+259del ENSP00000241256.2:n.796+208_796+259del
NM_198407.2:c.796+208_796+259del MANE Select NP_940799.1:n.796+208_796+259del
Search 100 bp 5'
Search 100 bp 3'