Canonical Allele Identifier: CA412975946
Gene: CYBB HGNC NCBI

Linked Data

dbSNP Id: rs1602179940

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37796005G>C , CM000685.2:g.37796005G>C GRCh38
NC_000023.10:g.37655258G>C , CM000685.1:g.37655258G>C GRCh37
NC_000023.9:g.37540198G>C NCBI36
NG_009065.1:g.20985G>C , LRG_53:g.20985G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696170.1:c.*47G>C ENSP00000512461.1:n.*47G>C
ENST00000696171.1:c.442G>C ENSP00000512462.1:p.Val148Leu
ENST00000696172.1:c.338-2950G>C ENSP00000512463.1:n.338-2950G>C
ENST00000378588.5:c.538G>C MANE Select ENSP00000367851.4:p.Val180Leu
ENST00000378588.4:c.538G>C ENSP00000367851.4:p.Val180Leu
ENST00000465127.1:c.171+370005G>C ENSP00000417050.1:n.171+370005G>C
NM_000397.3:c.538G>C , LRG_53t1:c.538G>C NP_000388.2:p.Val180Leu
XM_011543890.1:c.232G>C XP_011542192.1:p.Val78Leu
NM_000397.4:c.538G>C MANE Select NP_000388.2:p.Val180Leu