Canonical Allele Identifier: CA552611466
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1425910517
gnomAD v2: 4-68606455-G-C
MyVariant Identifiers: chr4:g.68606455G>C (hg19) chr4:g.67740737G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740737G>C , CM000666.2:g.67740737G>C GRCh38
NC_000004.11:g.68606455G>C , CM000666.1:g.68606455G>C GRCh37
NC_000004.10:g.68289050G>C NCBI36
NG_009293.1:g.20350C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.743-13C>G MANE Select ENSP00000226413.5:n.743-13C>G
ENST00000226413.4:c.743-13C>G ENSP00000226413.4:n.743-13C>G
ENST00000420975.2:c.615-13C>G ENSP00000397561.2:n.615-13C>G
NM_000406.2:c.743-13C>G NP_000397.1:n.743-13C>G
NM_001012763.1:c.615-13C>G NP_001012781.1:n.615-13C>G
NM_000406.3:c.743-13C>G MANE Select NP_000397.1:n.743-13C>G
NM_001012763.2:c.615-13C>G NP_001012781.1:n.615-13C>G
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