Canonical Allele Identifier: CA439924446
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740621-G-A
MyVariant Identifiers: chr4:g.68606339G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740621G>A , CM000666.2:g.67740621G>A GRCh38
NC_000004.11:g.68606339G>A , CM000666.1:g.68606339G>A GRCh37
NC_000004.10:g.68288934G>A NCBI36
NG_009293.1:g.20466C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.846C>T MANE Select ENSP00000226413.5:p.Pro282=
ENST00000226413.4:c.846C>T ENSP00000226413.4:p.Pro282=
ENST00000420975.2:c.718C>T ENSP00000397561.2:p.Leu240=
NM_000406.2:c.846C>T NP_000397.1:p.Pro282=
NM_001012763.1:c.718C>T NP_001012781.1:p.Leu240=
NM_000406.3:c.846C>T MANE Select NP_000397.1:p.Pro282=
NM_001012763.2:c.718C>T NP_001012781.1:p.Leu240=
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