Canonical Allele Identifier: CA2706125219
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs2109981051
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740333G>A , CM000666.2:g.67740333G>A GRCh38
NC_000004.11:g.68606051G>A , CM000666.1:g.68606051G>A GRCh37
NC_000004.10:g.68288646G>A NCBI36
NG_009293.1:g.20754C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*147C>T MANE Select ENSP00000226413.5:n.*147C>T
ENST00000226413.4:c.*147C>T ENSP00000226413.4:n.*147C>T
NM_000406.2:c.*147C>T NP_000397.1:n.*147C>T
NM_001012763.1:c.*256C>T NP_001012781.1:n.*256C>T
NM_000406.3:c.*147C>T MANE Select NP_000397.1:n.*147C>T
NM_001012763.2:c.*256C>T NP_001012781.1:n.*256C>T
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