Canonical Allele Identifier: CA1619112049

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356417_31356418delinsGT , CM000668.2:g.31356417_31356418delinsGT	GRCh38
NC_000006.11:g.31324194_31324195delinsGT , CM000668.1:g.31324194_31324195delinsGT	GRCh37
NC_000006.10:g.31432173_31432174delinsGT	NCBI36
NG_023187.1:g.5795_5796delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1841_1842delinsAC
ENST00000481849.6:n.1841_1842delinsAC
ENST00000497377.6:n.1841_1842delinsAC
ENST00000640094.2:c.368_369delinsAC	ENSP00000491275.2:p.Tyr123=
ENST00000696558.1:c.368_369delinsAC	ENSP00000512716.1:p.Tyr123=
ENST00000696559.1:c.368_369delinsAC	ENSP00000512717.1:p.Tyr123=
ENST00000696560.1:c.368_369delinsAC	ENSP00000512718.1:p.Tyr123=
ENST00000696561.1:c.368_369delinsAC	ENSP00000512719.1:p.Tyr123=
ENST00000696562.1:c.368_369delinsAC	ENSP00000512720.1:p.Tyr123=
ENST00000412585.7:c.368_369delinsAC MANE Select	ENSP00000399168.2:p.Tyr123=
ENST00000412585.6:c.368_369delinsAC	ENSP00000399168.2:p.Tyr123=
ENST00000434333.1:c.401_402delinsAC	ENSP00000405931.1:p.Tyr134=
ENST00000474381.1:n.243_244delinsAC
ENST00000498007.1:n.634_635delinsAC
NM_005514.6:c.368_369delinsAC	NP_005505.2:p.Tyr123=
XM_011514556.1:c.401_402delinsAC	XP_011512858.1:p.Tyr134=
XM_011514557.1:c.368_369delinsAC	XP_011512859.1:p.Tyr123=
XR_926175.1:n.378_379delinsAC
NM_005514.7:c.368_369delinsAC	NP_005505.2:p.Tyr123=
NM_005514.8:c.368_369delinsAC MANE Select	NP_005505.2:p.Tyr123=