Canonical Allele Identifier: CA2677957636
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356721_31356757del , CM000668.2:g.31356721_31356757del GRCh38
NC_000006.11:g.31324498_31324534del , CM000668.1:g.31324498_31324534del GRCh37
NC_000006.10:g.31432477_31432513del NCBI36
NG_023187.1:g.5457_5493del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1748_1784del
ENST00000481849.6:n.1748_1784del
ENST00000497377.6:n.1748_1784del
ENST00000640094.2:c.275_311del ENSP00000491275.2:p.Lys92ThrfsTer?
ENST00000696558.1:c.275_311del ENSP00000512716.1:p.Lys92ThrfsTer?
ENST00000696559.1:c.275_311del ENSP00000512717.1:p.Lys92ThrfsTer?
ENST00000696560.1:c.275_311del ENSP00000512718.1:p.Lys92ThrfsTer?
ENST00000696561.1:c.275_311del ENSP00000512719.1:p.Lys92ThrfsTer?
ENST00000696562.1:c.275_311del ENSP00000512720.1:p.Lys92ThrfsTer?
ENST00000412585.7:c.275_311del MANE Select ENSP00000399168.2:p.Lys92ThrfsTer?
ENST00000412585.6:c.275_311del ENSP00000399168.2:p.Lys92ThrfsTer?
ENST00000434333.1:c.308_344del ENSP00000405931.1:p.Lys103ThrfsTer?
ENST00000474381.1:n.150_186del
ENST00000498007.1:n.296_332del
ENST00000603274.1:n.75_111del
NM_005514.6:c.275_311del NP_005505.2:p.Lys92ThrfsTer?
XM_011514556.1:c.308_344del XP_011512858.1:p.Lys103ThrfsTer?
XM_011514557.1:c.275_311del XP_011512859.1:p.Lys92ThrfsTer?
XR_926175.1:n.285_321del
NM_005514.7:c.275_311del NP_005505.2:p.Lys92ThrfsTer?
NM_005514.8:c.275_311del MANE Select NP_005505.2:p.Lys92ThrfsTer?