Canonical Allele Identifier: CA1465421022
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754336A= , CM000666.2:g.67754336A= GRCh38
NC_000004.11:g.68620054A= , CM000666.1:g.68620054A= GRCh37
NC_000004.10:g.68302649A= NCBI36
NG_009293.1:g.6751T=

Transcript Alleles

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