Canonical Allele Identifier: CA2677957772

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356835-TCGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356836_31356838del , CM000668.2:g.31356836_31356838del	GRCh38
NC_000006.11:g.31324613_31324615del , CM000668.1:g.31324613_31324615del	GRCh37
NC_000006.10:g.31432592_31432594del	NCBI36
NG_023187.1:g.5375_5377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1666_1668del
ENST00000481849.6:n.1666_1668del
ENST00000497377.6:n.1666_1668del
ENST00000640094.2:c.193_195del	ENSP00000491275.2:p.Ala65del
ENST00000696558.1:c.193_195del	ENSP00000512716.1:p.Ala65del
ENST00000696559.1:c.193_195del	ENSP00000512717.1:p.Ala65del
ENST00000696560.1:c.193_195del	ENSP00000512718.1:p.Ala65del
ENST00000696561.1:c.193_195del	ENSP00000512719.1:p.Ala65del
ENST00000696562.1:c.193_195del	ENSP00000512720.1:p.Ala65del
ENST00000412585.7:c.193_195del MANE Select	ENSP00000399168.2:p.Ala65del
ENST00000412585.6:c.193_195del	ENSP00000399168.2:p.Ala65del
ENST00000434333.1:c.226_228del	ENSP00000405931.1:p.Ala76del
ENST00000474381.1:n.68_70del
ENST00000498007.1:n.214_216del
ENST00000603274.1:n.190_192del
NM_005514.6:c.193_195del	NP_005505.2:p.Ala65del
XM_011514556.1:c.226_228del	XP_011512858.1:p.Ala76del
XM_011514557.1:c.193_195del	XP_011512859.1:p.Ala65del
XR_926175.1:n.203_205del
NM_005514.7:c.193_195del	NP_005505.2:p.Ala65del
NM_005514.8:c.193_195del MANE Select	NP_005505.2:p.Ala65del