Canonical Allele Identifier: CA98672262
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs751972983
gnomAD v2: 4-68620043-C-G
gnomAD v3: 4-67754325-C-G
gnomAD v4: 4-67754325-C-G
MyVariant Identifiers: chr4:g.68620043C>G (hg19) chr4:g.67754325C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754325C>G , CM000666.2:g.67754325C>G GRCh38
NC_000004.11:g.68620043C>G , CM000666.1:g.68620043C>G GRCh37
NC_000004.10:g.68302638C>G NCBI36
NG_009293.1:g.6762G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.11G>C MANE Select ENSP00000226413.5:p.Ser4Thr
ENST00000226413.4:c.11G>C ENSP00000226413.4:p.Ser4Thr
ENST00000420975.2:c.11G>C ENSP00000397561.2:p.Ser4Thr
NM_000406.2:c.11G>C NP_000397.1:p.Ser4Thr
NM_001012763.1:c.11G>C NP_001012781.1:p.Ser4Thr
NM_000406.3:c.11G>C MANE Select NP_000397.1:p.Ser4Thr
NM_001012763.2:c.11G>C NP_001012781.1:p.Ser4Thr
Search 100 bp 5'
Search 100 bp 3'