Canonical Allele Identifier: CA2938930
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs148112458
ExAC: 4:68619587 C / T
gnomAD v2: 4-68619587-C-T
gnomAD v3: 4-67753869-C-T
gnomAD v4: 4-67753869-C-T
MyVariant Identifiers: chr4:g.68619587C>T (hg19) chr4:g.67753869C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753869C>T , CM000666.2:g.67753869C>T GRCh38
NC_000004.11:g.68619587C>T , CM000666.1:g.68619587C>T GRCh37
NC_000004.10:g.68302182C>T NCBI36
NG_009293.1:g.7218G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.467G>A MANE Select ENSP00000226413.5:p.Gly156Glu
ENST00000226413.4:c.467G>A ENSP00000226413.4:p.Gly156Glu
ENST00000420975.2:c.467G>A ENSP00000397561.2:p.Gly156Glu
NM_000406.2:c.467G>A NP_000397.1:p.Gly156Glu
NM_001012763.1:c.467G>A NP_001012781.1:p.Gly156Glu
NM_000406.3:c.467G>A MANE Select NP_000397.1:p.Gly156Glu
NM_001012763.2:c.467G>A NP_001012781.1:p.Gly156Glu
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