Canonical Allele Identifier: CA1619116785
Gene: HLA-B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359324G= , CM000668.2:g.31359324G= GRCh38
NC_000006.11:g.31327101G= , CM000668.1:g.31327101G= GRCh37
NC_000006.10:g.31435080G= NCBI36
NG_023187.1:g.2889C=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1271-1643C=
ENST00000481849.6:n.1271-1643C=
ENST00000497377.6:n.1271-1643C=
ENST00000696559.1:c.-203-1643C= ENSP00000512717.1:n.-203-1643C=
ENST00000696560.1:c.-203-1643C= ENSP00000512718.1:n.-203-1643C=
ENST00000696561.1:c.-203-1643C= ENSP00000512719.1:n.-203-1643C=
ENST00000696562.1:c.-135-2031C= ENSP00000512720.1:n.-135-2031C=
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