Canonical Allele Identifier: CA1087469653

Gene: HLA-B

Linked Data

• dbSNP Id: rs1767095224
• gnomAD v3: 6-31356772-T-TC
• gnomAD v4: 6-31356772-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356774dup , CM000668.2:g.31356774dup	GRCh38
NC_000006.11:g.31324551dup , CM000668.1:g.31324551dup	GRCh37
NC_000006.10:g.31432530dup	NCBI36
NG_023187.1:g.5440dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1731dup
ENST00000481849.6:n.1731dup
ENST00000497377.6:n.1731dup
ENST00000640094.2:c.258dup	ENSP00000491275.2:p.Asn87GlufsTer12
ENST00000696558.1:c.258dup	ENSP00000512716.1:p.Asn87GlufsTer12
ENST00000696559.1:c.258dup	ENSP00000512717.1:p.Asn87GlufsTer12
ENST00000696560.1:c.258dup	ENSP00000512718.1:p.Asn87GlufsTer12
ENST00000696561.1:c.258dup	ENSP00000512719.1:p.Asn87GlufsTer12
ENST00000696562.1:c.258dup	ENSP00000512720.1:p.Asn87GlufsTer12
ENST00000412585.7:c.258dup MANE Select	ENSP00000399168.2:p.Asn87GlufsTer12
ENST00000412585.6:c.258dup	ENSP00000399168.2:p.Asn87GlufsTer12
ENST00000434333.1:c.291dup	ENSP00000405931.1:p.Asn98GlufsTer12
ENST00000474381.1:n.133dup
ENST00000498007.1:n.279dup
ENST00000603274.1:n.128dup
NM_005514.6:c.258dup	NP_005505.2:p.Asn87GlufsTer12
XM_011514556.1:c.291dup	XP_011512858.1:p.Asn98GlufsTer12
XM_011514557.1:c.258dup	XP_011512859.1:p.Asn87GlufsTer12
XR_926175.1:n.268dup
NM_005514.7:c.258dup	NP_005505.2:p.Asn87GlufsTer12
NM_005514.8:c.258dup MANE Select	NP_005505.2:p.Asn87GlufsTer12