Canonical Allele Identifier: CA1697942205
Gene: GHRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30968991C= , CM000669.2:g.30968991C= GRCh38
NC_000007.13:g.31008606C= , CM000669.1:g.31008606C= GRCh37
NC_000007.12:g.30975131C= NCBI36
NG_021416.1:g.9971C=

Transcript Alleles

HGVS Amino-acid change
ENST00000326139.7:c.160+55C= MANE Select ENSP00000320180.2:n.160+55C=
ENST00000326139.6:c.160+55C= ENSP00000320180.2:n.160+55C=
NM_000823.3:c.160+55C= NP_000814.2:n.160+55C=
NM_000823.4:c.160+55C= MANE Select NP_000814.2:n.160+55C=
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