Canonical Allele Identifier: CA2939022
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs779455183
ExAC: 4:68620065 A / T
gnomAD v2: 4-68620065-A-T
gnomAD v3: 4-67754347-A-T
gnomAD v4: 4-67754347-A-T
MyVariant Identifiers: chr4:g.68620065A>T (hg19) chr4:g.67754347A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754347A>T , CM000666.2:g.67754347A>T GRCh38
NC_000004.11:g.68620065A>T , CM000666.1:g.68620065A>T GRCh37
NC_000004.10:g.68302660A>T NCBI36
NG_009293.1:g.6740T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-12T>A MANE Select ENSP00000226413.5:n.-12T>A
ENST00000226413.4:c.-12T>A ENSP00000226413.4:n.-12T>A
NM_000406.2:c.-12T>A NP_000397.1:n.-12T>A
NM_001012763.1:c.-12T>A NP_001012781.1:n.-12T>A
NM_000406.3:c.-12T>A MANE Select NP_000397.1:n.-12T>A
NM_001012763.2:c.-12T>A NP_001012781.1:n.-12T>A
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