Canonical Allele Identifier: CA1465408830
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs771419728
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740277A>C , CM000666.2:g.67740277A>C GRCh38
NC_000004.11:g.68605995A>C , CM000666.1:g.68605995A>C GRCh37
NC_000004.10:g.68288590A>C NCBI36
NG_009293.1:g.20810T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*203T>G MANE Select ENSP00000226413.5:n.*203T>G
ENST00000226413.4:c.*203T>G ENSP00000226413.4:n.*203T>G
NM_000406.2:c.*203T>G NP_000397.1:n.*203T>G
NM_001012763.1:c.*312T>G NP_001012781.1:n.*312T>G
NM_000406.3:c.*203T>G MANE Select NP_000397.1:n.*203T>G
NM_001012763.2:c.*312T>G NP_001012781.1:n.*312T>G
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