Canonical Allele Identifier: CA2424676617
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783831A= , CM000685.2:g.37783831A= GRCh38
NC_000023.10:g.37643084A= , CM000685.1:g.37643084A= GRCh37
NC_000023.9:g.37528028A= NCBI36
NG_009065.1:g.8815A= , LRG_53:g.8815A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.252+231A= ENSP00000512461.1:n.252+231A=
ENST00000696171.1:c.156+231A= ENSP00000512462.1:n.156+231A=
ENST00000696172.1:c.252+231A= ENSP00000512463.1:n.252+231A=
ENST00000696173.1:n.260+231A=
ENST00000378588.5:c.252+231A= MANE Select ENSP00000367851.4:n.252+231A=
ENST00000378588.4:c.252+231A= ENSP00000367851.4:n.252+231A=
ENST00000465127.1:c.171+357831A= ENSP00000417050.1:n.171+357831A=
NM_000397.3:c.252+231A= , LRG_53t1:c.252+231A= NP_000388.2:n.252+231A=
XM_011543890.1:c.-179+231A= XP_011542192.1:n.-179+231A=
NM_000397.4:c.252+231A= MANE Select NP_000388.2:n.252+231A=