Canonical Allele Identifier: CA98671975
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1023699758
gnomAD v4: 4-67753928-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753928G>A , CM000666.2:g.67753928G>A GRCh38
NC_000004.11:g.68619646G>A , CM000666.1:g.68619646G>A GRCh37
NC_000004.10:g.68302241G>A NCBI36
NG_009293.1:g.7159C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.408C>T MANE Select ENSP00000226413.5:p.Ser136=
ENST00000226413.4:c.408C>T ENSP00000226413.4:p.Ser136=
ENST00000420975.2:c.408C>T ENSP00000397561.2:p.Ser136=
NM_000406.2:c.408C>T NP_000397.1:p.Ser136=
NM_001012763.1:c.408C>T NP_001012781.1:p.Ser136=
NM_000406.3:c.408C>T MANE Select NP_000397.1:p.Ser136=
NM_001012763.2:c.408C>T NP_001012781.1:p.Ser136=