Canonical Allele Identifier: CA439933879
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619940T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754222T>C , CM000666.2:g.67754222T>C GRCh38
NC_000004.11:g.68619940T>C , CM000666.1:g.68619940T>C GRCh37
NC_000004.10:g.68302535T>C NCBI36
NG_009293.1:g.6865A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.114A>G MANE Select ENSP00000226413.5:p.Arg38=
ENST00000226413.4:c.114A>G ENSP00000226413.4:p.Arg38=
ENST00000420975.2:c.114A>G ENSP00000397561.2:p.Arg38=
NM_000406.2:c.114A>G NP_000397.1:p.Arg38=
NM_001012763.1:c.114A>G NP_001012781.1:p.Arg38=
NM_000406.3:c.114A>G MANE Select NP_000397.1:p.Arg38=
NM_001012763.2:c.114A>G NP_001012781.1:p.Arg38=