Canonical Allele Identifier: CA2578100703
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754369T>C , CM000666.2:g.67754369T>C GRCh38
NC_000004.11:g.68620087T>C , CM000666.1:g.68620087T>C GRCh37
NC_000004.10:g.68302682T>C NCBI36
NG_009293.1:g.6718A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-34A>G MANE Select ENSP00000226413.5:n.-34A>G
NM_000406.2:c.-34A>G NP_000397.1:n.-34A>G
NM_001012763.1:c.-34A>G NP_001012781.1:n.-34A>G
NM_000406.3:c.-34A>G MANE Select NP_000397.1:n.-34A>G
NM_001012763.2:c.-34A>G NP_001012781.1:n.-34A>G