Canonical Allele Identifier: CA10621554
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 349451
ClinVar RCV Id: RCV000368769
dbSNP Id: rs886059565
MyVariant Identifiers: chr4:g.68605849T>G (hg19) chr4:g.67740131T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740131T>G , CM000666.2:g.67740131T>G GRCh38
NC_000004.11:g.68605849T>G , CM000666.1:g.68605849T>G GRCh37
NC_000004.10:g.68288444T>G NCBI36
NG_009293.1:g.20956A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*349A>C MANE Select ENSP00000226413.5:n.*349A>C
ENST00000226413.4:c.*349A>C ENSP00000226413.4:n.*349A>C
NM_000406.2:c.*349A>C NP_000397.1:n.*349A>C
NM_001012763.1:c.*458A>C NP_001012781.1:n.*458A>C
NM_000406.3:c.*349A>C MANE Select NP_000397.1:n.*349A>C
NM_001012763.2:c.*458A>C NP_001012781.1:n.*458A>C
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