Canonical Allele Identifier: CA1465421028
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754353C= , CM000666.2:g.67754353C= GRCh38
NC_000004.11:g.68620071C= , CM000666.1:g.68620071C= GRCh37
NC_000004.10:g.68302666C= NCBI36
NG_009293.1:g.6734G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-18G= MANE Select ENSP00000226413.5:n.-18G=
ENST00000226413.4:c.-18G= ENSP00000226413.4:n.-18G=
NM_000406.2:c.-18G= NP_000397.1:n.-18G=
NM_001012763.1:c.-18G= NP_001012781.1:n.-18G=
NM_000406.3:c.-18G= MANE Select NP_000397.1:n.-18G=
NM_001012763.2:c.-18G= NP_001012781.1:n.-18G=