Canonical Allele Identifier: CA1619114219

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357110_31357111delinsGG , CM000668.2:g.31357110_31357111delinsGG	GRCh38
NC_000006.11:g.31324887_31324888delinsGG , CM000668.1:g.31324887_31324888delinsGG	GRCh37
NC_000006.10:g.31432866_31432867delinsGG	NCBI36
NG_023187.1:g.5102_5103delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1521_1522delinsCC
ENST00000481849.6:n.1521_1522delinsCC
ENST00000497377.6:n.1521_1522delinsCC
ENST00000640094.2:c.48_49delinsCC	ENSP00000491275.2:p.Ala16=
ENST00000696558.1:c.48_49delinsCC	ENSP00000512716.1:p.Ala16=
ENST00000696559.1:c.48_49delinsCC	ENSP00000512717.1:p.Ala16=
ENST00000696560.1:c.48_49delinsCC	ENSP00000512718.1:p.Ala16=
ENST00000696561.1:c.48_49delinsCC	ENSP00000512719.1:p.Ala16=
ENST00000696562.1:c.48_49delinsCC	ENSP00000512720.1:p.Ala16=
ENST00000412585.7:c.48_49delinsCC MANE Select	ENSP00000399168.2:p.Ala16=
ENST00000412585.6:c.48_49delinsCC	ENSP00000399168.2:p.Ala16=
ENST00000434333.1:c.-48_-47delinsCC	ENSP00000405931.1:n.-48_-47delinsCC
ENST00000498007.1:n.69_70delinsCC
ENST00000603274.1:n.464_465delinsGG
NM_005514.6:c.48_49delinsCC	NP_005505.2:p.Ala16=
XM_011514557.1:c.48_49delinsCC	XP_011512859.1:p.Ala16=
XR_926175.1:n.58_59delinsCC
NM_005514.7:c.48_49delinsCC	NP_005505.2:p.Ala16=
NM_005514.8:c.48_49delinsCC MANE Select	NP_005505.2:p.Ala16=