Canonical Allele Identifier: CA552611478

Gene: GNRHR

Linked Data

• dbSNP Id: rs1261120963
• gnomAD v2: 4-68620175-GTATGTCAAAT-G
• gnomAD v3: 4-67754457-GTATGTCAAAT-G
• gnomAD v4: 4-67754457-GTATGTCAAAT-G
• MyVariant Identifiers: chr4:g.68620176_68620185del (hg19) ; chr4:g.67754458_67754467del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754459_67754468del , CM000666.2:g.67754459_67754468del	GRCh38
NC_000004.11:g.68620177_68620186del , CM000666.1:g.68620177_68620186del	GRCh37
NC_000004.10:g.68302772_68302781del	NCBI36
NG_009293.1:g.6620_6629del

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-132_-123del	NP_000397.1:n.-132_-123del
NM_001012763.1:c.-132_-123del	NP_001012781.1:n.-132_-123del