Canonical Allele Identifier: CA552611454

Gene: GNRHR

Linked Data

• dbSNP Id: rs1017038022
• gnomAD v2: 4-68606187-T-G
• gnomAD v3: 4-67740469-T-G
• gnomAD v4: 4-67740469-T-G
• MyVariant Identifiers: chr4:g.68606187T>G (hg19) ; chr4:g.67740469T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740469T>G , CM000666.2:g.67740469T>G	GRCh38
NC_000004.11:g.68606187T>G , CM000666.1:g.68606187T>G	GRCh37
NC_000004.10:g.68288782T>G	NCBI36
NG_009293.1:g.20618A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*11A>C MANE Select	ENSP00000226413.5:n.*11A>C
ENST00000226413.4:c.*11A>C	ENSP00000226413.4:n.*11A>C
NM_000406.2:c.*11A>C	NP_000397.1:n.*11A>C
NM_001012763.1:c.*120A>C	NP_001012781.1:n.*120A>C
NM_000406.3:c.*11A>C MANE Select	NP_000397.1:n.*11A>C
NM_001012763.2:c.*120A>C	NP_001012781.1:n.*120A>C