Canonical Allele Identifier: CA439930665
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619652C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753934C>G , CM000666.2:g.67753934C>G GRCh38
NC_000004.11:g.68619652C>G , CM000666.1:g.68619652C>G GRCh37
NC_000004.10:g.68302247C>G NCBI36
NG_009293.1:g.7153G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.402G>C MANE Select ENSP00000226413.5:p.Val134=
ENST00000226413.4:c.402G>C ENSP00000226413.4:p.Val134=
ENST00000420975.2:c.402G>C ENSP00000397561.2:p.Val134=
NM_000406.2:c.402G>C NP_000397.1:p.Val134=
NM_001012763.1:c.402G>C NP_001012781.1:p.Val134=
NM_000406.3:c.402G>C MANE Select NP_000397.1:p.Val134=
NM_001012763.2:c.402G>C NP_001012781.1:p.Val134=
Search 100 bp 5'
Search 100 bp 3'