Canonical Allele Identifier: CA357048291
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606395T>C (hg19) chr4:g.67740677T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740677T>C , CM000666.2:g.67740677T>C GRCh38
NC_000004.11:g.68606395T>C , CM000666.1:g.68606395T>C GRCh37
NC_000004.10:g.68288990T>C NCBI36
NG_009293.1:g.20410A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.790A>G MANE Select ENSP00000226413.5:p.Lys264Glu
ENST00000226413.4:c.790A>G ENSP00000226413.4:p.Lys264Glu
ENST00000420975.2:c.662A>G ENSP00000397561.2:p.Glu221Gly
NM_000406.2:c.790A>G NP_000397.1:p.Lys264Glu
NM_001012763.1:c.662A>G NP_001012781.1:p.Glu221Gly
NM_000406.3:c.790A>G MANE Select NP_000397.1:p.Lys264Glu
NM_001012763.2:c.662A>G NP_001012781.1:p.Glu221Gly
Search 100 bp 5'
Search 100 bp 3'