Canonical Allele Identifier: CA2939030

Gene: GNRHR

Linked Data

• dbSNP Id: rs769880332
• ExAC: 4:68620093 G / A
• gnomAD v2: 4-68620093-G-A
• gnomAD v4: 4-67754375-G-A
• MyVariant Identifiers: chr4:g.68620093G>A (hg19) ; chr4:g.67754375G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754375G>A , CM000666.2:g.67754375G>A	GRCh38
NC_000004.11:g.68620093G>A , CM000666.1:g.68620093G>A	GRCh37
NC_000004.10:g.68302688G>A	NCBI36
NG_009293.1:g.6712C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.-40C>T MANE Select	ENSP00000226413.5:n.-40C>T
NM_000406.2:c.-40C>T	NP_000397.1:n.-40C>T
NM_001012763.1:c.-40C>T	NP_001012781.1:n.-40C>T
NM_000406.3:c.-40C>T MANE Select	NP_000397.1:n.-40C>T
NM_001012763.2:c.-40C>T	NP_001012781.1:n.-40C>T