Canonical Allele Identifier: CA1465421034
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs748014023
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754362T>A , CM000666.2:g.67754362T>A GRCh38
NC_000004.11:g.68620080T>A , CM000666.1:g.68620080T>A GRCh37
NC_000004.10:g.68302675T>A NCBI36
NG_009293.1:g.6725A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-27A>T MANE Select ENSP00000226413.5:n.-27A>T
NM_000406.2:c.-27A>T NP_000397.1:n.-27A>T
NM_001012763.1:c.-27A>T NP_001012781.1:n.-27A>T
NM_000406.3:c.-27A>T MANE Select NP_000397.1:n.-27A>T
NM_001012763.2:c.-27A>T NP_001012781.1:n.-27A>T
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