Canonical Allele Identifier: CA136833479

Gene: HLA-B

Linked Data

• dbSNP Id: rs45516893
• MyVariant Identifiers: chr6:g.31323943del (hg19) ; chr6:g.31356166del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356167del , CM000668.2:g.31356167del	GRCh38
NC_000006.11:g.31323944del , CM000668.1:g.31323944del	GRCh37
NC_000006.10:g.31431923del	NCBI36
NG_023187.1:g.6047del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2093del
ENST00000481849.6:n.2092+1del
ENST00000497377.6:n.2092+1del
ENST00000640094.2:c.619+1del
ENST00000696558.1:c.619+1del
ENST00000696559.1:c.619+1del
ENST00000696560.1:c.619+1del
ENST00000696561.1:c.619+1del
ENST00000696562.1:c.619+1del
ENST00000412585.7:c.619+1del
ENST00000412585.6:c.619+1del
ENST00000434333.1:c.652+1del
ENST00000474381.1:n.495del
ENST00000498007.1:n.885+1del
NM_005514.6:c.619+1del
XM_011514556.1:c.652+1del
XM_011514557.1:c.619+1del
XR_926175.1:n.630del
NM_005514.7:c.619+1del
NM_005514.8:c.619+1del