Canonical Allele Identifier: CA1619114641
Gene: HLA-B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357315A= , CM000668.2:g.31357315A= GRCh38
NC_000006.11:g.31325092A= , CM000668.1:g.31325092A= GRCh37
NC_000006.10:g.31433071A= NCBI36
NG_023187.1:g.4898T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-22T=
ENST00000481849.6:n.1339-22T=
ENST00000497377.6:n.1339-22T=
ENST00000696559.1:c.-135-22T= ENSP00000512717.1:n.-135-22T=
ENST00000696560.1:c.-135-22T= ENSP00000512718.1:n.-135-22T=
ENST00000696561.1:c.-135-22T= ENSP00000512719.1:n.-135-22T=
ENST00000696562.1:c.-135-22T= ENSP00000512720.1:n.-135-22T=
ENST00000603274.1:n.669A=
XR_926692.1:n.165-22T=
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