Canonical Allele Identifier: CA2693426679
Gene: CYBB HGNC NCBI

Linked Data

gnomAD v4: X-37804281-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37804281T>C , CM000685.2:g.37804281T>C GRCh38
NC_000023.10:g.37663534T>C , CM000685.1:g.37663534T>C GRCh37
NC_000023.9:g.37548478T>C NCBI36
NG_009065.1:g.29265T>C , LRG_53:g.29265T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.*660+151T>C ENSP00000512461.1:n.*660+151T>C
ENST00000696171.1:c.1055+151T>C ENSP00000512462.1:n.1055+151T>C
ENST00000378588.5:c.1151+151T>C MANE Select ENSP00000367851.4:n.1151+151T>C
ENST00000378588.4:c.1151+151T>C ENSP00000367851.4:n.1151+151T>C
ENST00000465127.1:c.171+378281T>C ENSP00000417050.1:n.171+378281T>C
NM_000397.3:c.1151+151T>C , LRG_53t1:c.1151+151T>C NP_000388.2:n.1151+151T>C
XM_011543890.1:c.845+151T>C XP_011542192.1:n.845+151T>C
NM_000397.4:c.1151+151T>C MANE Select NP_000388.2:n.1151+151T>C
Search 100 bp 5'
Search 100 bp 3'