Canonical Allele Identifier: CA2670819712
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740327-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740327T>C , CM000666.2:g.67740327T>C GRCh38
NC_000004.11:g.68606045T>C , CM000666.1:g.68606045T>C GRCh37
NC_000004.10:g.68288640T>C NCBI36
NG_009293.1:g.20760A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.*153A>G MANE Select ENSP00000226413.5:n.*153A>G
ENST00000226413.4:c.*153A>G ENSP00000226413.4:n.*153A>G
NM_000406.2:c.*153A>G NP_000397.1:n.*153A>G
NM_001012763.1:c.*262A>G NP_001012781.1:n.*262A>G
NM_000406.3:c.*153A>G MANE Select NP_000397.1:n.*153A>G
NM_001012763.2:c.*262A>G NP_001012781.1:n.*262A>G
Search 100 bp 5'
Search 100 bp 3'