Canonical Allele Identifier: CA1697942198
Gene: GHRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30968981T= , CM000669.2:g.30968981T= GRCh38
NC_000007.13:g.31008596T= , CM000669.1:g.31008596T= GRCh37
NC_000007.12:g.30975121T= NCBI36
NG_021416.1:g.9961T=

Transcript Alleles

HGVS Amino-acid change
ENST00000326139.7:c.160+45T= MANE Select ENSP00000320180.2:n.160+45T=
ENST00000326139.6:c.160+45T= ENSP00000320180.2:n.160+45T=
NM_000823.3:c.160+45T= NP_000814.2:n.160+45T=
NM_000823.4:c.160+45T= MANE Select NP_000814.2:n.160+45T=
Search 100 bp 5'
Search 100 bp 3'