Canonical Allele Identifier: CA357047439
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs754571423
gnomAD v3: 4-67740554-T-C
gnomAD v4: 4-67740554-T-C
MyVariant Identifiers: chr4:g.68606272T>C (hg19) chr4:g.67740554T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740554T>C , CM000666.2:g.67740554T>C GRCh38
NC_000004.11:g.68606272T>C , CM000666.1:g.68606272T>C GRCh37
NC_000004.10:g.68288867T>C NCBI36
NG_009293.1:g.20533A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.913A>G MANE Select ENSP00000226413.5:p.Asn305Asp
ENST00000226413.4:c.913A>G ENSP00000226413.4:p.Asn305Asp
ENST00000420975.2:c.785A>G ENSP00000397561.2:n.785A>G
NM_000406.2:c.913A>G NP_000397.1:p.Asn305Asp
NM_001012763.1:c.*35A>G NP_001012781.1:n.*35A>G
NM_000406.3:c.913A>G MANE Select NP_000397.1:p.Asn305Asp
NM_001012763.2:c.*35A>G NP_001012781.1:n.*35A>G
Search 100 bp 5'
Search 100 bp 3'