Canonical Allele Identifier: CA1465420345
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731912259
gnomAD v4: 4-67753736-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753736T>C , CM000666.2:g.67753736T>C GRCh38
NC_000004.11:g.68619454T>C , CM000666.1:g.68619454T>C GRCh37
NC_000004.10:g.68302049T>C NCBI36
NG_009293.1:g.7351A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.522+78A>G MANE Select ENSP00000226413.5:n.522+78A>G
ENST00000226413.4:c.522+78A>G ENSP00000226413.4:n.522+78A>G
ENST00000420975.2:c.522+78A>G ENSP00000397561.2:n.522+78A>G
NM_000406.2:c.522+78A>G NP_000397.1:n.522+78A>G
NM_001012763.1:c.522+78A>G NP_001012781.1:n.522+78A>G
NM_000406.3:c.522+78A>G MANE Select NP_000397.1:n.522+78A>G
NM_001012763.2:c.522+78A>G NP_001012781.1:n.522+78A>G
Search 100 bp 5'
Search 100 bp 3'