Canonical Allele Identifier: CA1619116701
Gene: HLA-B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359201A= , CM000668.2:g.31359201A= GRCh38
NC_000006.11:g.31326978A= , CM000668.1:g.31326978A= GRCh37
NC_000006.10:g.31434957A= NCBI36
NG_023187.1:g.3012T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1271-1520T=
ENST00000481849.6:n.1271-1520T=
ENST00000497377.6:n.1271-1520T=
ENST00000696559.1:c.-203-1520T= ENSP00000512717.1:n.-203-1520T=
ENST00000696560.1:c.-203-1520T= ENSP00000512718.1:n.-203-1520T=
ENST00000696561.1:c.-203-1520T= ENSP00000512719.1:n.-203-1520T=
ENST00000696562.1:c.-135-1908T= ENSP00000512720.1:n.-135-1908T=
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