Canonical Allele Identifier: CA2670819690
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740283-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740283T>G , CM000666.2:g.67740283T>G GRCh38
NC_000004.11:g.68606001T>G , CM000666.1:g.68606001T>G GRCh37
NC_000004.10:g.68288596T>G NCBI36
NG_009293.1:g.20804A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*197A>C MANE Select ENSP00000226413.5:n.*197A>C
ENST00000226413.4:c.*197A>C ENSP00000226413.4:n.*197A>C
NM_000406.2:c.*197A>C NP_000397.1:n.*197A>C
NM_001012763.1:c.*306A>C NP_001012781.1:n.*306A>C
NM_000406.3:c.*197A>C MANE Select NP_000397.1:n.*197A>C
NM_001012763.2:c.*306A>C NP_001012781.1:n.*306A>C
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