Canonical Allele Identifier: CA439924353
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740585-A-G
MyVariant Identifiers: chr4:g.68606303A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740585A>G , CM000666.2:g.67740585A>G GRCh38
NC_000004.11:g.68606303A>G , CM000666.1:g.68606303A>G GRCh37
NC_000004.10:g.68288898A>G NCBI36
NG_009293.1:g.20502T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.882T>C MANE Select ENSP00000226413.5:p.Pro294=
ENST00000226413.4:c.882T>C ENSP00000226413.4:p.Pro294=
ENST00000420975.2:c.754T>C ENSP00000397561.2:n.754T>C
NM_000406.2:c.882T>C NP_000397.1:p.Pro294=
NM_001012763.1:c.*4T>C NP_001012781.1:n.*4T>C
NM_000406.3:c.882T>C MANE Select NP_000397.1:p.Pro294=
NM_001012763.2:c.*4T>C NP_001012781.1:n.*4T>C
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