Canonical Allele Identifier: CA2839056796
Gene: GHRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30969018C>A , CM000669.2:g.30969018C>A GRCh38
NC_000007.13:g.31008633C>A , CM000669.1:g.31008633C>A GRCh37
NC_000007.12:g.30975158C>A NCBI36
NG_021416.1:g.9998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326139.7:c.161-45C>A MANE Select ENSP00000320180.2:n.161-45C>A
ENST00000326139.6:c.161-45C>A ENSP00000320180.2:n.161-45C>A
NM_000823.3:c.161-45C>A NP_000814.2:n.161-45C>A
NM_000823.4:c.161-45C>A MANE Select NP_000814.2:n.161-45C>A
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