Canonical Allele Identifier: CA439931491
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1469253300
gnomAD v2: 4-68619793-G-A
gnomAD v3: 4-67754075-G-A
gnomAD v4: 4-67754075-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754075G>A , CM000666.2:g.67754075G>A GRCh38
NC_000004.11:g.68619793G>A , CM000666.1:g.68619793G>A GRCh37
NC_000004.10:g.68302388G>A NCBI36
NG_009293.1:g.7012C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.261C>T MANE Select ENSP00000226413.5:p.Asn87=
ENST00000226413.4:c.261C>T ENSP00000226413.4:p.Asn87=
ENST00000420975.2:c.261C>T ENSP00000397561.2:p.Asn87=
NM_000406.2:c.261C>T NP_000397.1:p.Asn87=
NM_001012763.1:c.261C>T NP_001012781.1:p.Asn87=
NM_000406.3:c.261C>T MANE Select NP_000397.1:p.Asn87=
NM_001012763.2:c.261C>T NP_001012781.1:p.Asn87=