Canonical Allele Identifier: CA2939026
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs748014023
ExAC: 4:68620080 T / G
gnomAD v2: 4-68620080-T-G
gnomAD v4: 4-67754362-T-G
MyVariant Identifiers: chr4:g.68620080T>G (hg19) chr4:g.67754362T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754362T>G , CM000666.2:g.67754362T>G GRCh38
NC_000004.11:g.68620080T>G , CM000666.1:g.68620080T>G GRCh37
NC_000004.10:g.68302675T>G NCBI36
NG_009293.1:g.6725A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-27A>C MANE Select ENSP00000226413.5:n.-27A>C
NM_000406.2:c.-27A>C NP_000397.1:n.-27A>C
NM_001012763.1:c.-27A>C NP_001012781.1:n.-27A>C
NM_000406.3:c.-27A>C MANE Select NP_000397.1:n.-27A>C
NM_001012763.2:c.-27A>C NP_001012781.1:n.-27A>C
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