Canonical Allele Identifier: CA573469483
Gene: GHRHR HGNC NCBI

Linked Data

dbSNP Id: rs1489670918
gnomAD v2: 7-31008587-A-G
gnomAD v4: 7-30968972-A-G
MyVariant Identifiers: chr7:g.31008587A>G (hg19) chr7:g.30968972A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30968972A>G , CM000669.2:g.30968972A>G GRCh38
NC_000007.13:g.31008587A>G , CM000669.1:g.31008587A>G GRCh37
NC_000007.12:g.30975112A>G NCBI36
NG_021416.1:g.9952A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000326139.7:c.160+36A>G MANE Select ENSP00000320180.2:n.160+36A>G
ENST00000326139.6:c.160+36A>G ENSP00000320180.2:n.160+36A>G
NM_000823.3:c.160+36A>G NP_000814.2:n.160+36A>G
NM_000823.4:c.160+36A>G MANE Select NP_000814.2:n.160+36A>G
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