Canonical Allele Identifier: CA439930798

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68619682G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753964G>C , CM000666.2:g.67753964G>C	GRCh38
NC_000004.11:g.68619682G>C , CM000666.1:g.68619682G>C	GRCh37
NC_000004.10:g.68302277G>C	NCBI36
NG_009293.1:g.7123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.372C>G MANE Select	ENSP00000226413.5:p.Ser124=
ENST00000226413.4:c.372C>G	ENSP00000226413.4:p.Ser124=
ENST00000420975.2:c.372C>G	ENSP00000397561.2:p.Ser124=
NM_000406.2:c.372C>G	NP_000397.1:p.Ser124=
NM_001012763.1:c.372C>G	NP_001012781.1:p.Ser124=
NM_000406.3:c.372C>G MANE Select	NP_000397.1:p.Ser124=
NM_001012763.2:c.372C>G	NP_001012781.1:p.Ser124=