Canonical Allele Identifier: CA357056897
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs775721426
gnomAD v2: 4-68620040-G-T
gnomAD v4: 4-67754322-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754322G>T , CM000666.2:g.67754322G>T GRCh38
NC_000004.11:g.68620040G>T , CM000666.1:g.68620040G>T GRCh37
NC_000004.10:g.68302635G>T NCBI36
NG_009293.1:g.6765C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.14C>A MANE Select ENSP00000226413.5:p.Ala5Asp
ENST00000226413.4:c.14C>A ENSP00000226413.4:p.Ala5Asp
ENST00000420975.2:c.14C>A ENSP00000397561.2:p.Ala5Asp
NM_000406.2:c.14C>A NP_000397.1:p.Ala5Asp
NM_001012763.1:c.14C>A NP_001012781.1:p.Ala5Asp
NM_000406.3:c.14C>A MANE Select NP_000397.1:p.Ala5Asp
NM_001012763.2:c.14C>A NP_001012781.1:p.Ala5Asp