Canonical Allele Identifier: CA1697966110
Gene: GHRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30979358G= , CM000669.2:g.30979358G= GRCh38
NC_000007.13:g.31018973G= , CM000669.1:g.31018973G= GRCh37
NC_000007.12:g.30985498G= NCBI36
NG_021416.1:g.20338G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326139.7:c.*114G= MANE Select ENSP00000320180.2:n.*114G=
ENST00000326139.6:c.*114G= ENSP00000320180.2:n.*114G=
ENST00000337750.9:c.*602G= ENSP00000338184.4:n.*602G=
ENST00000396227.6:c.*602G= ENSP00000379529.2:n.*602G=
ENST00000409316.5:c.*229G= ENSP00000386602.1:n.*229G=
ENST00000409904.7:c.*114G= ENSP00000387113.3:n.*114G=
ENST00000461424.5:n.680+2800G=
ENST00000463164.1:n.370G=
ENST00000611037.1:c.550+2800G= ENSP00000480159.1:n.550+2800G=
NM_000823.3:c.*114G= NP_000814.2:n.*114G=
XM_011515263.1:c.*114G= XP_011513565.1:n.*114G=
NM_000823.4:c.*114G= MANE Select NP_000814.2:n.*114G=