Canonical Allele Identifier: CA2670819631
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740152-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740152C>A , CM000666.2:g.67740152C>A GRCh38
NC_000004.11:g.68605870C>A , CM000666.1:g.68605870C>A GRCh37
NC_000004.10:g.68288465C>A NCBI36
NG_009293.1:g.20935G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*328G>T MANE Select ENSP00000226413.5:n.*328G>T
ENST00000226413.4:c.*328G>T ENSP00000226413.4:n.*328G>T
NM_000406.2:c.*328G>T NP_000397.1:n.*328G>T
NM_001012763.1:c.*437G>T NP_001012781.1:n.*437G>T
NM_000406.3:c.*328G>T MANE Select NP_000397.1:n.*328G>T
NM_001012763.2:c.*437G>T NP_001012781.1:n.*437G>T
Search 100 bp 5'
Search 100 bp 3'