Canonical Allele Identifier: CA552156795
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1368712627
gnomAD v2: 4-68605937-A-C
gnomAD v3: 4-67740219-A-C
gnomAD v4: 4-67740219-A-C
MyVariant Identifiers: chr4:g.68605937A>C (hg19) chr4:g.67740219A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740219A>C , CM000666.2:g.67740219A>C GRCh38
NC_000004.11:g.68605937A>C , CM000666.1:g.68605937A>C GRCh37
NC_000004.10:g.68288532A>C NCBI36
NG_009293.1:g.20868T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*261T>G MANE Select ENSP00000226413.5:n.*261T>G
ENST00000226413.4:c.*261T>G ENSP00000226413.4:n.*261T>G
NM_000406.2:c.*261T>G NP_000397.1:n.*261T>G
NM_001012763.1:c.*370T>G NP_001012781.1:n.*370T>G
NM_000406.3:c.*261T>G MANE Select NP_000397.1:n.*261T>G
NM_001012763.2:c.*370T>G NP_001012781.1:n.*370T>G
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