Canonical Allele Identifier: CA357056933

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67754328-T-C
• MyVariant Identifiers: chr4:g.68620046T>C (hg19) ; chr4:g.67754328T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754328T>C , CM000666.2:g.67754328T>C	GRCh38
NC_000004.11:g.68620046T>C , CM000666.1:g.68620046T>C	GRCh37
NC_000004.10:g.68302641T>C	NCBI36
NG_009293.1:g.6759A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.8A>G MANE Select	ENSP00000226413.5:p.Asn3Ser
ENST00000226413.4:c.8A>G	ENSP00000226413.4:p.Asn3Ser
ENST00000420975.2:c.8A>G	ENSP00000397561.2:p.Asn3Ser
NM_000406.2:c.8A>G	NP_000397.1:p.Asn3Ser
NM_001012763.1:c.8A>G	NP_001012781.1:p.Asn3Ser
NM_000406.3:c.8A>G MANE Select	NP_000397.1:p.Asn3Ser
NM_001012763.2:c.8A>G	NP_001012781.1:p.Asn3Ser