Canonical Allele Identifier: CA1697966145
Gene: GHRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30979366T= , CM000669.2:g.30979366T= GRCh38
NC_000007.13:g.31018981T= , CM000669.1:g.31018981T= GRCh37
NC_000007.12:g.30985506T= NCBI36
NG_021416.1:g.20346T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000326139.7:c.*122T= MANE Select ENSP00000320180.2:n.*122T=
ENST00000326139.6:c.*122T= ENSP00000320180.2:n.*122T=
ENST00000337750.9:c.*610T= ENSP00000338184.4:n.*610T=
ENST00000396227.6:c.*610T= ENSP00000379529.2:n.*610T=
ENST00000409316.5:c.*237T= ENSP00000386602.1:n.*237T=
ENST00000409904.7:c.*122T= ENSP00000387113.3:n.*122T=
ENST00000461424.5:n.680+2808T=
ENST00000463164.1:n.378T=
ENST00000611037.1:c.550+2808T= ENSP00000480159.1:n.550+2808T=
NM_000823.3:c.*122T= NP_000814.2:n.*122T=
XM_011515263.1:c.*122T= XP_011513565.1:n.*122T=
NM_000823.4:c.*122T= MANE Select NP_000814.2:n.*122T=