Canonical Allele Identifier: CA357047393
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606261G>C (hg19) chr4:g.67740543G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740543G>C , CM000666.2:g.67740543G>C GRCh38
NC_000004.11:g.68606261G>C , CM000666.1:g.68606261G>C GRCh37
NC_000004.10:g.68288856G>C NCBI36
NG_009293.1:g.20544C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.924C>G MANE Select ENSP00000226413.5:p.Phe308Leu
ENST00000226413.4:c.924C>G ENSP00000226413.4:p.Phe308Leu
ENST00000420975.2:c.796C>G ENSP00000397561.2:n.796C>G
NM_000406.2:c.924C>G NP_000397.1:p.Phe308Leu
NM_001012763.1:c.*46C>G NP_001012781.1:n.*46C>G
NM_000406.3:c.924C>G MANE Select NP_000397.1:p.Phe308Leu
NM_001012763.2:c.*46C>G NP_001012781.1:n.*46C>G
Search 100 bp 5'
Search 100 bp 3'