Canonical Allele Identifier: CA552611507
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1370093348
gnomAD v2: 4-68619481-T-C
gnomAD v4: 4-67753763-T-C
MyVariant Identifiers: chr4:g.68619481T>C (hg19) chr4:g.67753763T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753763T>C , CM000666.2:g.67753763T>C GRCh38
NC_000004.11:g.68619481T>C , CM000666.1:g.68619481T>C GRCh37
NC_000004.10:g.68302076T>C NCBI36
NG_009293.1:g.7324A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.522+51A>G MANE Select ENSP00000226413.5:n.522+51A>G
ENST00000226413.4:c.522+51A>G ENSP00000226413.4:n.522+51A>G
ENST00000420975.2:c.522+51A>G ENSP00000397561.2:n.522+51A>G
NM_000406.2:c.522+51A>G NP_000397.1:n.522+51A>G
NM_001012763.1:c.522+51A>G NP_001012781.1:n.522+51A>G
NM_000406.3:c.522+51A>G MANE Select NP_000397.1:n.522+51A>G
NM_001012763.2:c.522+51A>G NP_001012781.1:n.522+51A>G
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