Canonical Allele Identifier: CA2939024
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs754624617
ExAC: 4:68620071 C / T
gnomAD v2: 4-68620071-C-T
MyVariant Identifiers: chr4:g.68620071C>T (hg19) chr4:g.67754353C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754353C>T , CM000666.2:g.67754353C>T GRCh38
NC_000004.11:g.68620071C>T , CM000666.1:g.68620071C>T GRCh37
NC_000004.10:g.68302666C>T NCBI36
NG_009293.1:g.6734G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-18G>A MANE Select ENSP00000226413.5:n.-18G>A
ENST00000226413.4:c.-18G>A ENSP00000226413.4:n.-18G>A
NM_000406.2:c.-18G>A NP_000397.1:n.-18G>A
NM_001012763.1:c.-18G>A NP_001012781.1:n.-18G>A
NM_000406.3:c.-18G>A MANE Select NP_000397.1:n.-18G>A
NM_001012763.2:c.-18G>A NP_001012781.1:n.-18G>A
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