Canonical Allele Identifier: CA2578564584

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357039-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357041_31357042dup , CM000668.2:g.31357041_31357042dup	GRCh38
NC_000006.11:g.31324818_31324819dup , CM000668.1:g.31324818_31324819dup	GRCh37
NC_000006.10:g.31432797_31432798dup	NCBI36
NG_023187.1:g.5172_5173dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+45_1546+46dup
ENST00000481849.6:n.1546+45_1546+46dup
ENST00000497377.6:n.1546+45_1546+46dup
ENST00000640094.2:c.73+45_73+46dup	ENSP00000491275.2:n.73+45_73+46dup
ENST00000696558.1:c.73+45_73+46dup	ENSP00000512716.1:n.73+45_73+46dup
ENST00000696559.1:c.73+45_73+46dup	ENSP00000512717.1:n.73+45_73+46dup
ENST00000696560.1:c.73+45_73+46dup	ENSP00000512718.1:n.73+45_73+46dup
ENST00000696561.1:c.73+45_73+46dup	ENSP00000512719.1:n.73+45_73+46dup
ENST00000696562.1:c.73+45_73+46dup	ENSP00000512720.1:n.73+45_73+46dup
ENST00000412585.7:c.73+45_73+46dup MANE Select	ENSP00000399168.2:n.73+45_73+46dup
ENST00000412585.6:c.73+45_73+46dup	ENSP00000399168.2:n.73+45_73+46dup
ENST00000434333.1:c.23_24dup	ENSP00000405931.1:p.Gly9ArgfsTer?
ENST00000498007.1:n.94+45_94+46dup
ENST00000603274.1:n.395_396dup
NM_005514.6:c.73+45_73+46dup	NP_005505.2:n.73+45_73+46dup
XM_011514556.1:c.23_24dup	XP_011512858.1:p.Gly9ArgfsTer?
XM_011514557.1:c.73+45_73+46dup	XP_011512859.1:n.73+45_73+46dup
XR_926175.1:n.83+45_83+46dup
NM_005514.7:c.73+45_73+46dup	NP_005505.2:n.73+45_73+46dup
NM_005514.8:c.73+45_73+46dup MANE Select	NP_005505.2:n.73+45_73+46dup