Canonical Allele Identifier: CA136836779

Gene: HLA-B

Linked Data

• dbSNP Id: rs151341069
• MyVariant Identifiers: chr6:g.31325087del (hg19) ; chr6:g.31357310del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357310del , CM000668.2:g.31357310del	GRCh38
NC_000006.11:g.31325087del , CM000668.1:g.31325087del	GRCh37
NC_000006.10:g.31433066del	NCBI36
NG_023187.1:g.4903del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1339-17del
ENST00000481849.6:n.1339-17del
ENST00000497377.6:n.1339-17del
ENST00000696559.1:c.-135-17del	ENSP00000512717.1:n.-135-17del
ENST00000696560.1:c.-135-17del	ENSP00000512718.1:n.-135-17del
ENST00000696561.1:c.-135-17del	ENSP00000512719.1:n.-135-17del
ENST00000696562.1:c.-135-17del	ENSP00000512720.1:n.-135-17del
ENST00000603274.1:n.664del
XR_926692.1:n.165-17del