Canonical Allele Identifier: CA2677955107
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355219_31355242del , CM000668.2:g.31355219_31355242del GRCh38
NC_000006.11:g.31322996_31323019del , CM000668.1:g.31322996_31323019del GRCh37
NC_000006.10:g.31430975_31430998del NCBI36
NG_023187.1:g.6978_7001del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2943-12_2954del
ENST00000481849.6:n.2450_2473del
ENST00000497377.6:n.2369-12_2380del
ENST00000640094.2:c.895+82_895+105del ENSP00000491275.2:n.895+82_895+105del
ENST00000696558.1:c.965-12_976del
ENST00000696559.1:c.896-12_907del
ENST00000696560.1:c.896-12_907del
ENST00000696561.1:c.896-12_907del
ENST00000696562.1:c.896-12_907del
ENST00000412585.7:c.896-12_907del
ENST00000640094.1:c.88+82_88+105del ENSP00000491275.1:n.88+82_88+105del
ENST00000412585.6:c.896-12_907del
ENST00000463574.1:n.487-12_498del
NM_005514.6:c.896-12_907del
XM_011514556.1:c.929-12_940del
XM_011514557.1:c.895+82_895+105del XP_011512859.1:n.895+82_895+105del
XR_926175.1:n.1335-12_1346del
NM_005514.7:c.896-12_907del
NM_005514.8:c.896-12_907del