Canonical Allele Identifier: CA1619113056

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356762_31356763delinsAT , CM000668.2:g.31356762_31356763delinsAT	GRCh38
NC_000006.11:g.31324539_31324540delinsAT , CM000668.1:g.31324539_31324540delinsAT	GRCh37
NC_000006.10:g.31432518_31432519delinsAT	NCBI36
NG_023187.1:g.5450_5451delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1741_1742delinsAT
ENST00000481849.6:n.1741_1742delinsAT
ENST00000497377.6:n.1741_1742delinsAT
ENST00000640094.2:c.268_269delinsAT	ENSP00000491275.2:p.Ile90=
ENST00000696558.1:c.268_269delinsAT	ENSP00000512716.1:p.Ile90=
ENST00000696559.1:c.268_269delinsAT	ENSP00000512717.1:p.Ile90=
ENST00000696560.1:c.268_269delinsAT	ENSP00000512718.1:p.Ile90=
ENST00000696561.1:c.268_269delinsAT	ENSP00000512719.1:p.Ile90=
ENST00000696562.1:c.268_269delinsAT	ENSP00000512720.1:p.Ile90=
ENST00000412585.7:c.268_269delinsAT MANE Select	ENSP00000399168.2:p.Ile90=
ENST00000412585.6:c.268_269delinsAT	ENSP00000399168.2:p.Ile90=
ENST00000434333.1:c.301_302delinsAT	ENSP00000405931.1:p.Ile101=
ENST00000474381.1:n.143_144delinsAT
ENST00000498007.1:n.289_290delinsAT
ENST00000603274.1:n.116_117delinsAT
NM_005514.6:c.268_269delinsAT	NP_005505.2:p.Ile90=
XM_011514556.1:c.301_302delinsAT	XP_011512858.1:p.Ile101=
XM_011514557.1:c.268_269delinsAT	XP_011512859.1:p.Ile90=
XR_926175.1:n.278_279delinsAT
NM_005514.7:c.268_269delinsAT	NP_005505.2:p.Ile90=
NM_005514.8:c.268_269delinsAT MANE Select	NP_005505.2:p.Ile90=