Canonical Allele Identifier: CA9847459
Gene: GHRH HGNC NCBI

Linked Data

dbSNP Id: rs4988492

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.37254295G>A , CM000682.2:g.37254295G>A GRCh38
NC_000020.10:g.35882698G>A , CM000682.1:g.35882698G>A GRCh37
NC_000020.9:g.35316112G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000237527.8:c.223C>T ENSP00000237527.4:p.Leu75Phe
ENST00000373614.7:c.223C>T MANE Select ENSP00000362716.2:p.Leu75Phe
ENST00000237527.7:c.223C>T ENSP00000237527.3:p.Leu75Phe
ENST00000373611.2:c.223C>T ENSP00000362713.2:p.Leu75Phe
ENST00000373614.6:c.223C>T ENSP00000362716.2:p.Leu75Phe
NM_001184731.1:c.223C>T NP_001171660.1:p.Leu75Phe
NM_021081.4:c.223C>T NP_066567.1:p.Leu75Phe
XM_011528784.1:c.223C>T XP_011527086.1:p.Leu75Phe
XM_011528785.1:c.223C>T XP_011527087.1:p.Leu75Phe
XM_011528786.1:c.223C>T XP_011527088.1:p.Leu75Phe
XM_011528787.1:c.223C>T XP_011527089.1:p.Leu75Phe
XM_011528788.1:c.223C>T XP_011527090.1:p.Leu75Phe
NM_001184731.2:c.223C>T NP_001171660.1:p.Leu75Phe
NM_021081.5:c.223C>T NP_066567.1:p.Leu75Phe
XM_011528784.2:c.223C>T XP_011527086.1:p.Leu75Phe
XM_011528788.2:c.223C>T XP_011527090.1:p.Leu75Phe
NM_001184731.3:c.223C>T NP_001171660.1:p.Leu75Phe
NM_021081.6:c.223C>T MANE Select NP_066567.1:p.Leu75Phe