Canonical Allele Identifier: CA2939025

Gene: GNRHR

Linked Data

• dbSNP Id: rs778827924
• ExAC: 4:68620079 C / G
• gnomAD v2: 4-68620079-C-G
• gnomAD v3: 4-67754361-C-G
• gnomAD v4: 4-67754361-C-G
• MyVariant Identifiers: chr4:g.68620079C>G (hg19) ; chr4:g.67754361C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754361C>G , CM000666.2:g.67754361C>G	GRCh38
NC_000004.11:g.68620079C>G , CM000666.1:g.68620079C>G	GRCh37
NC_000004.10:g.68302674C>G	NCBI36
NG_009293.1:g.6726G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.-26G>C MANE Select	ENSP00000226413.5:n.-26G>C
NM_000406.2:c.-26G>C	NP_000397.1:n.-26G>C
NM_001012763.1:c.-26G>C	NP_001012781.1:n.-26G>C
NM_000406.3:c.-26G>C MANE Select	NP_000397.1:n.-26G>C
NM_001012763.2:c.-26G>C	NP_001012781.1:n.-26G>C