Canonical Allele Identifier: CA1619114511
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357224G= , CM000668.2:g.31357224G= GRCh38
NC_000006.11:g.31325001G= , CM000668.1:g.31325001G= GRCh37
NC_000006.10:g.31432980G= NCBI36
NG_023187.1:g.4989C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1408C=
ENST00000481849.6:n.1408C=
ENST00000497377.6:n.1408C=
ENST00000696559.1:c.-66C= ENSP00000512717.1:n.-66C=
ENST00000696560.1:c.-66C= ENSP00000512718.1:n.-66C=
ENST00000696561.1:c.-66C= ENSP00000512719.1:n.-66C=
ENST00000696562.1:c.-66C= ENSP00000512720.1:n.-66C=
ENST00000603274.1:n.578G=
NM_005514.7:c.-66C= NP_005505.2:n.-66C=