Canonical Allele Identifier: CA2668560004
Gene: GHSR HGNC NCBI

Linked Data

gnomAD v4: 3-172447382-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447382G>T , CM000665.2:g.172447382G>T GRCh38
NC_000003.11:g.172165172G>T , CM000665.1:g.172165172G>T GRCh37
NC_000003.10:g.173647866G>T NCBI36
NG_021159.1:g.6075C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+236C>A MANE Select ENSP00000241256.2:n.796+236C>A
ENST00000241256.2:c.796+236C>A ENSP00000241256.2:n.796+236C>A
NM_198407.2:c.796+236C>A MANE Select NP_940799.1:n.796+236C>A
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