Canonical Allele Identifier: CA2840383832

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356971_31356972insT , CM000668.2:g.31356971_31356972insT	GRCh38
NC_000006.11:g.31324748_31324749insT , CM000668.1:g.31324748_31324749insT	GRCh37
NC_000006.10:g.31432727_31432728insT	NCBI36
NG_023187.1:g.5241_5242insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1547-15_1547-14insA
ENST00000481849.6:n.1547-15_1547-14insA
ENST00000497377.6:n.1547-15_1547-14insA
ENST00000640094.2:c.74-15_74-14insA	ENSP00000491275.2:n.74-15_74-14insA
ENST00000696558.1:c.74-15_74-14insA	ENSP00000512716.1:n.74-15_74-14insA
ENST00000696559.1:c.74-15_74-14insA	ENSP00000512717.1:n.74-15_74-14insA
ENST00000696560.1:c.74-15_74-14insA	ENSP00000512718.1:n.74-15_74-14insA
ENST00000696561.1:c.74-15_74-14insA	ENSP00000512719.1:n.74-15_74-14insA
ENST00000696562.1:c.74-15_74-14insA	ENSP00000512720.1:n.74-15_74-14insA
ENST00000412585.7:c.74-15_74-14insA MANE Select	ENSP00000399168.2:n.74-15_74-14insA
ENST00000412585.6:c.74-15_74-14insA	ENSP00000399168.2:n.74-15_74-14insA
ENST00000434333.1:c.92_93insA	ENSP00000405931.1:p.Ser32LeufsTer?
ENST00000498007.1:n.95-15_95-14insA
ENST00000603274.1:n.325_326insT
NM_005514.6:c.74-15_74-14insA	NP_005505.2:n.74-15_74-14insA
XM_011514556.1:c.92_93insA	XP_011512858.1:p.Ser32LeufsTer?
XM_011514557.1:c.74-15_74-14insA	XP_011512859.1:n.74-15_74-14insA
XR_926175.1:n.84-15_84-14insA
NM_005514.7:c.74-15_74-14insA	NP_005505.2:n.74-15_74-14insA
NM_005514.8:c.74-15_74-14insA MANE Select	NP_005505.2:n.74-15_74-14insA