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ClinGen Allele Registry
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Canonical Allele Identifier:
CA1396711258
Community Standard Title: NC_000003.12:g.119780660T=
Gene: NR1I2
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.119780660T= , CM000665.2:g.119780660T=
GRCh38
NC_000003.11:g.119499507T= , CM000665.1:g.119499507T=
GRCh37
NC_000003.10:g.120982197T=
NCBI36
NG_011856.1:g.5177T=
Transcript Alleles
HGVS
Amino-acid Change
NM_003889.3:c.-1663T=
NP_003880.3:n.-1663T=
NM_033013.2:c.-1663T=
NP_148934.1:n.-1663T=
ENST00000393716.6:c.-1663T=
ENSP00000377319.2:n.-1663T=
ENST00000466380.5:c.-1663T=
ENSP00000420297.1:n.-1663T=
ENST00000466380.6:c.-1663T=
ENSP00000420297.2:n.-1663T=
ENST00000648112.1:c.*2-26569T=
ENSP00000497876.1:n.*2-26569T=
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