Canonical Allele Identifier: CA357047572
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740586-G-T
MyVariant Identifiers: chr4:g.68606304G>T (hg19) chr4:g.67740586G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740586G>T , CM000666.2:g.67740586G>T GRCh38
NC_000004.11:g.68606304G>T , CM000666.1:g.68606304G>T GRCh37
NC_000004.10:g.68288899G>T NCBI36
NG_009293.1:g.20501C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.881C>A MANE Select ENSP00000226413.5:p.Pro294His
ENST00000226413.4:c.881C>A ENSP00000226413.4:p.Pro294His
ENST00000420975.2:c.753C>A ENSP00000397561.2:n.753C>A
NM_000406.2:c.881C>A NP_000397.1:p.Pro294His
NM_001012763.1:c.*3C>A NP_001012781.1:n.*3C>A
NM_000406.3:c.881C>A MANE Select NP_000397.1:p.Pro294His
NM_001012763.2:c.*3C>A NP_001012781.1:n.*3C>A
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