Canonical Allele Identifier: CA357048609

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68606444T>C (hg19) ; chr4:g.67740726T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740726T>C , CM000666.2:g.67740726T>C	GRCh38
NC_000004.11:g.68606444T>C , CM000666.1:g.68606444T>C	GRCh37
NC_000004.10:g.68289039T>C	NCBI36
NG_009293.1:g.20361A>G

Transcript Alleles

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