Canonical Allele Identifier: CA1619116433
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354052G= , CM000668.2:g.31354052G= GRCh38
NC_000006.11:g.31321829G= , CM000668.1:g.31321829G= GRCh37
NC_000006.10:g.31429808G= NCBI36
NG_023187.1:g.8161C=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3385C=
ENST00000481849.6:n.3345C=
ENST00000497377.6:n.3252C=
ENST00000696558.1:c.1407C= ENSP00000512716.1:n.1407C=
ENST00000696559.1:c.*249C= ENSP00000512717.1:n.*249C=
ENST00000696560.1:c.*249C= ENSP00000512718.1:n.*249C=
ENST00000696561.1:c.*249C= ENSP00000512719.1:n.*249C=
ENST00000696562.1:c.*249C= ENSP00000512720.1:n.*249C=
ENST00000412585.7:c.*249C= MANE Select ENSP00000399168.2:n.*249C=
ENST00000412585.6:c.*249C= ENSP00000399168.2:n.*249C=
ENST00000481849.5:n.573C=
ENST00000497377.5:n.737C=
NM_005514.6:c.*249C= NP_005505.2:n.*249C=
XM_011514556.1:c.*249C= XP_011512858.1:n.*249C=
XM_011514557.1:c.*249C= XP_011512859.1:n.*249C=
XR_926175.1:n.1777C=
NM_005514.7:c.*249C= NP_005505.2:n.*249C=
NM_005514.8:c.*249C= MANE Select NP_005505.2:n.*249C=