Canonical Allele Identifier: CA2670820629
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754360-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754360C>A , CM000666.2:g.67754360C>A GRCh38
NC_000004.11:g.68620078C>A , CM000666.1:g.68620078C>A GRCh37
NC_000004.10:g.68302673C>A NCBI36
NG_009293.1:g.6727G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-25G>T MANE Select ENSP00000226413.5:n.-25G>T
ENST00000226413.4:c.-25G>T ENSP00000226413.4:n.-25G>T
NM_000406.2:c.-25G>T NP_000397.1:n.-25G>T
NM_001012763.1:c.-25G>T NP_001012781.1:n.-25G>T
NM_000406.3:c.-25G>T MANE Select NP_000397.1:n.-25G>T
NM_001012763.2:c.-25G>T NP_001012781.1:n.-25G>T
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