Canonical Allele Identifier: CA1465420351
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753740T= , CM000666.2:g.67753740T= GRCh38
NC_000004.11:g.68619458T= , CM000666.1:g.68619458T= GRCh37
NC_000004.10:g.68302053T= NCBI36
NG_009293.1:g.7347A=

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.522+74A= MANE Select ENSP00000226413.5:n.522+74A=
ENST00000226413.4:c.522+74A= ENSP00000226413.4:n.522+74A=
ENST00000420975.2:c.522+74A= ENSP00000397561.2:n.522+74A=
NM_000406.2:c.522+74A= NP_000397.1:n.522+74A=
NM_001012763.1:c.522+74A= NP_001012781.1:n.522+74A=
NM_000406.3:c.522+74A= MANE Select NP_000397.1:n.522+74A=
NM_001012763.2:c.522+74A= NP_001012781.1:n.522+74A=
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