Canonical Allele Identifier: CA439933636
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754135-T-C
MyVariant Identifiers: chr4:g.68619853T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754135T>C , CM000666.2:g.67754135T>C GRCh38
NC_000004.11:g.68619853T>C , CM000666.1:g.68619853T>C GRCh37
NC_000004.10:g.68302448T>C NCBI36
NG_009293.1:g.6952A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.201A>G MANE Select ENSP00000226413.5:p.Lys67=
ENST00000226413.4:c.201A>G ENSP00000226413.4:p.Lys67=
ENST00000420975.2:c.201A>G ENSP00000397561.2:p.Lys67=
NM_000406.2:c.201A>G NP_000397.1:p.Lys67=
NM_001012763.1:c.201A>G NP_001012781.1:p.Lys67=
NM_000406.3:c.201A>G MANE Select NP_000397.1:p.Lys67=
NM_001012763.2:c.201A>G NP_001012781.1:p.Lys67=
Search 100 bp 5'
Search 100 bp 3'