Canonical Allele Identifier: CA98667346
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs59079898
MyVariant Identifiers: chr4:g.67740113G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740113G>C , CM000666.2:g.67740113G>C GRCh38
NC_000004.11:g.68605831G>C , CM000666.1:g.68605831G>C GRCh37
NC_000004.10:g.68288426G>C NCBI36
NG_009293.1:g.20974C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*367C>G MANE Select ENSP00000226413.5:n.*367C>G
ENST00000226413.4:c.*367C>G ENSP00000226413.4:n.*367C>G
NM_000406.2:c.*367C>G NP_000397.1:n.*367C>G
NM_001012763.1:c.*476C>G NP_001012781.1:n.*476C>G
NM_000406.3:c.*367C>G MANE Select NP_000397.1:n.*367C>G
NM_001012763.2:c.*476C>G NP_001012781.1:n.*476C>G
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