Canonical Allele Identifier: CA2579582948
Gene: CYBB HGNC NCBI

Linked Data

gnomAD v4: X-37795902-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37795902G>C , CM000685.2:g.37795902G>C GRCh38
NC_000023.10:g.37655155G>C , CM000685.1:g.37655155G>C GRCh37
NC_000023.9:g.37540095G>C NCBI36
NG_009065.1:g.20882G>C , LRG_53:g.20882G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696170.1:c.338-49G>C ENSP00000512461.1:n.338-49G>C
ENST00000696171.1:c.388-49G>C ENSP00000512462.1:n.388-49G>C
ENST00000696172.1:c.338-3053G>C ENSP00000512463.1:n.338-3053G>C
ENST00000378588.5:c.484-49G>C MANE Select ENSP00000367851.4:n.484-49G>C
ENST00000378588.4:c.484-49G>C ENSP00000367851.4:n.484-49G>C
ENST00000465127.1:c.171+369902G>C ENSP00000417050.1:n.171+369902G>C
NM_000397.3:c.484-49G>C , LRG_53t1:c.484-49G>C NP_000388.2:n.484-49G>C
XM_011543890.1:c.178-49G>C XP_011542192.1:n.178-49G>C
NM_000397.4:c.484-49G>C MANE Select NP_000388.2:n.484-49G>C
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