Canonical Allele Identifier: CA2654283626
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026320-GGTGCAT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026325_33026330del , CM000683.2:g.33026325_33026330del GRCh38
NC_000021.8:g.34398633_34398638del , CM000683.1:g.34398633_34398638del GRCh37
NC_000021.7:g.33320503_33320508del NCBI36
NG_011834.1:g.5395_5400del

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+299_-63+304del MANE Select ENSP00000371794.3:n.-63+299_-63+304del
ENST00000333337.3:c.-538_-533del ENSP00000331040.3:n.-538_-533del
ENST00000382357.3:c.-63+299_-63+304del ENSP00000371794.3:n.-63+299_-63+304del
ENST00000430860.1:c.-63+65_-63+70del ENSP00000391183.1:n.-63+65_-63+70del
NM_005806.3:c.-63+299_-63+304del NP_005797.1:n.-63+299_-63+304del
XM_005260908.1:c.-63+65_-63+70del XP_005260965.1:n.-63+65_-63+70del
NM_005806.4:c.-63+299_-63+304del MANE Select NP_005797.1:n.-63+299_-63+304del
Search 100 bp 5'
Search 100 bp 3'