Canonical Allele Identifier: CA2938937
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs182806311
ExAC: 4:68619599 T / C
gnomAD v2: 4-68619599-T-C
gnomAD v3: 4-67753881-T-C
gnomAD v4: 4-67753881-T-C
MyVariant Identifiers: chr4:g.68619599T>C (hg19) chr4:g.67753881T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753881T>C , CM000666.2:g.67753881T>C GRCh38
NC_000004.11:g.68619599T>C , CM000666.1:g.68619599T>C GRCh37
NC_000004.10:g.68302194T>C NCBI36
NG_009293.1:g.7206A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.455A>G MANE Select ENSP00000226413.5:p.Asn152Ser
ENST00000226413.4:c.455A>G ENSP00000226413.4:p.Asn152Ser
ENST00000420975.2:c.455A>G ENSP00000397561.2:p.Asn152Ser
NM_000406.2:c.455A>G NP_000397.1:p.Asn152Ser
NM_001012763.1:c.455A>G NP_001012781.1:p.Asn152Ser
NM_000406.3:c.455A>G MANE Select NP_000397.1:p.Asn152Ser
NM_001012763.2:c.455A>G NP_001012781.1:p.Asn152Ser
Search 100 bp 5'
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