Canonical Allele Identifier: CA797693228
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1235378015
gnomAD v3: 4-67740149-G-T
gnomAD v4: 4-67740149-G-T
MyVariant Identifiers: chr4:g.68605867G>T (hg19) chr4:g.67740149G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740149G>T , CM000666.2:g.67740149G>T GRCh38
NC_000004.11:g.68605867G>T , CM000666.1:g.68605867G>T GRCh37
NC_000004.10:g.68288462G>T NCBI36
NG_009293.1:g.20938C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*331C>A MANE Select ENSP00000226413.5:n.*331C>A
ENST00000226413.4:c.*331C>A ENSP00000226413.4:n.*331C>A
NM_000406.2:c.*331C>A NP_000397.1:n.*331C>A
NM_001012763.1:c.*440C>A NP_001012781.1:n.*440C>A
NM_000406.3:c.*331C>A MANE Select NP_000397.1:n.*331C>A
NM_001012763.2:c.*440C>A NP_001012781.1:n.*440C>A
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