Canonical Allele Identifier: CA552611445
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1159448395
gnomAD v2: 4-68606158-C-T
gnomAD v4: 4-67740440-C-T
MyVariant Identifiers: chr4:g.68606158C>T (hg19) chr4:g.67740440C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740440C>T , CM000666.2:g.67740440C>T GRCh38
NC_000004.11:g.68606158C>T , CM000666.1:g.68606158C>T GRCh37
NC_000004.10:g.68288753C>T NCBI36
NG_009293.1:g.20647G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*40G>A MANE Select ENSP00000226413.5:n.*40G>A
ENST00000226413.4:c.*40G>A ENSP00000226413.4:n.*40G>A
NM_000406.2:c.*40G>A NP_000397.1:n.*40G>A
NM_001012763.1:c.*149G>A NP_001012781.1:n.*149G>A
NM_000406.3:c.*40G>A MANE Select NP_000397.1:n.*40G>A
NM_001012763.2:c.*149G>A NP_001012781.1:n.*149G>A
Search 100 bp 5'
Search 100 bp 3'