Canonical Allele Identifier: CA439933857
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619913C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754195C>T , CM000666.2:g.67754195C>T GRCh38
NC_000004.11:g.68619913C>T , CM000666.1:g.68619913C>T GRCh37
NC_000004.10:g.68302508C>T NCBI36
NG_009293.1:g.6892G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.141G>A MANE Select ENSP00000226413.5:p.Leu47=
ENST00000226413.4:c.141G>A ENSP00000226413.4:p.Leu47=
ENST00000420975.2:c.141G>A ENSP00000397561.2:p.Leu47=
NM_000406.2:c.141G>A NP_000397.1:p.Leu47=
NM_001012763.1:c.141G>A NP_001012781.1:p.Leu47=
NM_000406.3:c.141G>A MANE Select NP_000397.1:p.Leu47=
NM_001012763.2:c.141G>A NP_001012781.1:p.Leu47=
Search 100 bp 5'
Search 100 bp 3'