Canonical Allele Identifier: CA98667402

Gene: GNRHR

Linked Data

• ClinVar Variation Id: 904090
• ClinVar RCV Id: RCV001151793
• dbSNP Id: rs529064600
• gnomAD v2: 4-68606005-T-C
• gnomAD v3: 4-67740287-T-C
• gnomAD v4: 4-67740287-T-C
• MyVariant Identifiers: chr4:g.68606005T>C (hg19) ; chr4:g.67740287T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740287T>C , CM000666.2:g.67740287T>C	GRCh38
NC_000004.11:g.68606005T>C , CM000666.1:g.68606005T>C	GRCh37
NC_000004.10:g.68288600T>C	NCBI36
NG_009293.1:g.20800A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*193A>G MANE Select	ENSP00000226413.5:n.*193A>G
ENST00000226413.4:c.*193A>G	ENSP00000226413.4:n.*193A>G
NM_000406.2:c.*193A>G	NP_000397.1:n.*193A>G
NM_001012763.1:c.*302A>G	NP_001012781.1:n.*302A>G
NM_000406.3:c.*193A>G MANE Select	NP_000397.1:n.*193A>G
NM_001012763.2:c.*302A>G	NP_001012781.1:n.*302A>G