Canonical Allele Identifier: CA357047998
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740646-G-T
MyVariant Identifiers: chr4:g.68606364G>T (hg19) chr4:g.67740646G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740646G>T , CM000666.2:g.67740646G>T GRCh38
NC_000004.11:g.68606364G>T , CM000666.1:g.68606364G>T GRCh37
NC_000004.10:g.68288959G>T NCBI36
NG_009293.1:g.20441C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.821C>A MANE Select ENSP00000226413.5:p.Thr274Asn
ENST00000226413.4:c.821C>A ENSP00000226413.4:p.Thr274Asn
ENST00000420975.2:c.693C>A ENSP00000397561.2:p.His231Gln
NM_000406.2:c.821C>A NP_000397.1:p.Thr274Asn
NM_001012763.1:c.693C>A NP_001012781.1:p.His231Gln
NM_000406.3:c.821C>A MANE Select NP_000397.1:p.Thr274Asn
NM_001012763.2:c.693C>A NP_001012781.1:p.His231Gln
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