Canonical Allele Identifier: CA439931032
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619727A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754009A>T , CM000666.2:g.67754009A>T GRCh38
NC_000004.11:g.68619727A>T , CM000666.1:g.68619727A>T GRCh37
NC_000004.10:g.68302322A>T NCBI36
NG_009293.1:g.7078T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.327T>A MANE Select ENSP00000226413.5:p.Ala109=
ENST00000226413.4:c.327T>A ENSP00000226413.4:p.Ala109=
ENST00000420975.2:c.327T>A ENSP00000397561.2:p.Ala109=
NM_000406.2:c.327T>A NP_000397.1:p.Ala109=
NM_001012763.1:c.327T>A NP_001012781.1:p.Ala109=
NM_000406.3:c.327T>A MANE Select NP_000397.1:p.Ala109=
NM_001012763.2:c.327T>A NP_001012781.1:p.Ala109=