Canonical Allele Identifier: CA2578564580
Gene: HLA-B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356652_31356654del , CM000668.2:g.31356652_31356654del GRCh38
NC_000006.11:g.31324429_31324431del , CM000668.1:g.31324429_31324431del GRCh37
NC_000006.10:g.31432408_31432410del NCBI36
NG_023187.1:g.5560_5562del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1816+35_1816+37del
ENST00000481849.6:n.1816+35_1816+37del
ENST00000497377.6:n.1816+35_1816+37del
ENST00000640094.2:c.343+35_343+37del ENSP00000491275.2:n.343+35_343+37del
ENST00000696558.1:c.343+35_343+37del ENSP00000512716.1:n.343+35_343+37del
ENST00000696559.1:c.343+35_343+37del ENSP00000512717.1:n.343+35_343+37del
ENST00000696560.1:c.343+35_343+37del ENSP00000512718.1:n.343+35_343+37del
ENST00000696561.1:c.343+35_343+37del ENSP00000512719.1:n.343+35_343+37del
ENST00000696562.1:c.343+35_343+37del ENSP00000512720.1:n.343+35_343+37del
ENST00000412585.7:c.343+35_343+37del MANE Select ENSP00000399168.2:n.343+35_343+37del
ENST00000412585.6:c.343+35_343+37del ENSP00000399168.2:n.343+35_343+37del
ENST00000434333.1:c.376+35_376+37del ENSP00000405931.1:n.376+35_376+37del
ENST00000474381.1:n.218+35_218+37del
ENST00000498007.1:n.399_401del
ENST00000603274.1:n.6_8del
NM_005514.6:c.343+35_343+37del NP_005505.2:n.343+35_343+37del
XM_011514556.1:c.376+35_376+37del XP_011512858.1:n.376+35_376+37del
XM_011514557.1:c.343+35_343+37del XP_011512859.1:n.343+35_343+37del
XR_926175.1:n.353+35_353+37del
NM_005514.7:c.343+35_343+37del NP_005505.2:n.343+35_343+37del
NM_005514.8:c.343+35_343+37del MANE Select NP_005505.2:n.343+35_343+37del
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