Canonical Allele Identifier: CA439928971

Gene: GNRHR

Linked Data

• dbSNP Id: rs1342562329
• gnomAD v2: 4-68619556-G-C
• MyVariant Identifiers: chr4:g.68619556G>C (hg19) ; chr4:g.67753838G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753838G>C , CM000666.2:g.67753838G>C	GRCh38
NC_000004.11:g.68619556G>C , CM000666.1:g.68619556G>C	GRCh37
NC_000004.10:g.68302151G>C	NCBI36
NG_009293.1:g.7249C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.498C>G MANE Select	ENSP00000226413.5:p.Leu166=
ENST00000226413.4:c.498C>G	ENSP00000226413.4:p.Leu166=
ENST00000420975.2:c.498C>G	ENSP00000397561.2:p.Leu166=
NM_000406.2:c.498C>G	NP_000397.1:p.Leu166=
NM_001012763.1:c.498C>G	NP_001012781.1:p.Leu166=
NM_000406.3:c.498C>G MANE Select	NP_000397.1:p.Leu166=
NM_001012763.2:c.498C>G	NP_001012781.1:p.Leu166=