Canonical Allele Identifier: CA650785881
Gene: HLA-B HGNC NCBI

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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354030_31354031insA , CM000668.2:g.31354030_31354031insA GRCh38
NC_000006.11:g.31321807_31321808insA , CM000668.1:g.31321807_31321808insA GRCh37
NC_000006.10:g.31429786_31429787insA NCBI36
NG_023187.1:g.8182_8183insT

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3406_3407insT
ENST00000481849.6:n.3366_3367insT
ENST00000497377.6:n.3273_3274insT
ENST00000696558.1:c.1428_1429insT ENSP00000512716.1:n.1428_1429insT
ENST00000696559.1:c.*270_*271insT ENSP00000512717.1:n.*270_*271insT
ENST00000696560.1:c.*270_*271insT ENSP00000512718.1:n.*270_*271insT
ENST00000696561.1:c.*270_*271insT ENSP00000512719.1:n.*270_*271insT
ENST00000696562.1:c.*270_*271insT ENSP00000512720.1:n.*270_*271insT
ENST00000412585.7:c.*270_*271insT MANE Select ENSP00000399168.2:n.*270_*271insT
ENST00000412585.6:c.*270_*271insT ENSP00000399168.2:n.*270_*271insT
ENST00000481849.5:n.594_595insT
ENST00000497377.5:n.758_759insT
NM_005514.6:c.*270_*271insT NP_005505.2:n.*270_*271insT
XM_011514556.1:c.*270_*271insT XP_011512858.1:n.*270_*271insT
XM_011514557.1:c.*270_*271insT XP_011512859.1:n.*270_*271insT
XR_926175.1:n.1798_1799insT
NM_005514.7:c.*270_*271insT NP_005505.2:n.*270_*271insT
NM_005514.8:c.*270_*271insT MANE Select NP_005505.2:n.*270_*271insT
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