Canonical Allele Identifier: CA1056402222
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1737487968
gnomAD v3: 3-172447382-G-A
gnomAD v4: 3-172447382-G-A
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+236C>T MANE Select ENSP00000241256.2:n.796+236C>T
ENST00000241256.2:c.796+236C>T ENSP00000241256.2:n.796+236C>T
NM_198407.2:c.796+236C>T MANE Select NP_940799.1:n.796+236C>T
Search 100 bp 5'
Search 100 bp 3'