Canonical Allele Identifier: CA14438255
Gene: CYB561 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63432917C>T , CM000679.2:g.63432917C>T GRCh38
NC_000017.10:g.61510278C>T , CM000679.1:g.61510278C>T GRCh37
NC_000017.9:g.58864010C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360793.8:c.*1485G>A MANE Select ENSP00000354028.3:n.*1485G>A
ENST00000360793.7:c.*1485G>A ENSP00000354028.3:n.*1485G>A
ENST00000392975.6:c.*1485G>A ENSP00000376701.2:n.*1485G>A
ENST00000392976.5:c.*1485G>A ENSP00000376702.1:n.*1485G>A
ENST00000584031.5:c.*1703G>A ENSP00000463162.1:n.*1703G>A
NM_001017916.1:c.*1485G>A NP_001017916.1:n.*1485G>A
NM_001017917.1:c.*1485G>A NP_001017917.1:n.*1485G>A
NM_001915.3:c.*1485G>A NP_001906.3:n.*1485G>A
XM_005257091.1:c.*1485G>A XP_005257148.1:n.*1485G>A
XM_011524424.1:c.*1583G>A XP_011522726.1:n.*1583G>A
NM_001330421.1:c.*1485G>A NP_001317350.1:n.*1485G>A
XM_017024261.2:c.*1583G>A XP_016879750.2:n.*1583G>A
XM_017024262.1:c.*1485G>A XP_016879751.1:n.*1485G>A
NM_001915.4:c.*1485G>A MANE Select NP_001906.3:n.*1485G>A
NM_001017917.2:c.*1485G>A NP_001017917.1:n.*1485G>A
NM_001330421.2:c.*1485G>A NP_001317350.1:n.*1485G>A
NM_001017916.2:c.*1485G>A NP_001017916.1:n.*1485G>A
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