Canonical Allele Identifier: CA2939013

Gene: GNRHR

Linked Data

• dbSNP Id: rs765234140
• ExAC: 4:68620039 G / T
• gnomAD v2: 4-68620039-G-T
• gnomAD v3: 4-67754321-G-T
• gnomAD v4: 4-67754321-G-T
• MyVariant Identifiers: chr4:g.68620039G>T (hg19) ; chr4:g.67754321G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754321G>T , CM000666.2:g.67754321G>T	GRCh38
NC_000004.11:g.68620039G>T , CM000666.1:g.68620039G>T	GRCh37
NC_000004.10:g.68302634G>T	NCBI36
NG_009293.1:g.6766C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.15C>A MANE Select	ENSP00000226413.5:p.Ala5=
ENST00000226413.4:c.15C>A	ENSP00000226413.4:p.Ala5=
ENST00000420975.2:c.15C>A	ENSP00000397561.2:p.Ala5=
NM_000406.2:c.15C>A	NP_000397.1:p.Ala5=
NM_001012763.1:c.15C>A	NP_001012781.1:p.Ala5=
NM_000406.3:c.15C>A MANE Select	NP_000397.1:p.Ala5=
NM_001012763.2:c.15C>A	NP_001012781.1:p.Ala5=