Canonical Allele Identifier: CA1087467983

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356370-T-TGCC
• gnomAD v4: 6-31356370-T-TGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356371_31356372insCCG , CM000668.2:g.31356371_31356372insCCG	GRCh38
NC_000006.11:g.31324148_31324149insCCG , CM000668.1:g.31324148_31324149insCCG	GRCh37
NC_000006.10:g.31432127_31432128insCCG	NCBI36
NG_023187.1:g.5842_5843insGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1888_1889insGGC
ENST00000481849.6:n.1888_1889insGGC
ENST00000497377.6:n.1888_1889insGGC
ENST00000640094.2:c.415_416insGGC	ENSP00000491275.2:p.Asp138_Gln139insArg
ENST00000696558.1:c.415_416insGGC	ENSP00000512716.1:p.Asp138_Gln139insArg
ENST00000696559.1:c.415_416insGGC	ENSP00000512717.1:p.Asp138_Gln139insArg
ENST00000696560.1:c.415_416insGGC	ENSP00000512718.1:p.Asp138_Gln139insArg
ENST00000696561.1:c.415_416insGGC	ENSP00000512719.1:p.Asp138_Gln139insArg
ENST00000696562.1:c.415_416insGGC	ENSP00000512720.1:p.Asp138_Gln139insArg
ENST00000412585.7:c.415_416insGGC MANE Select	ENSP00000399168.2:p.Asp138_Gln139insArg
ENST00000412585.6:c.415_416insGGC	ENSP00000399168.2:p.Asp138_Gln139insArg
ENST00000434333.1:c.448_449insGGC	ENSP00000405931.1:p.Asp149_Gln150insArg
ENST00000474381.1:n.290_291insGGC
ENST00000498007.1:n.681_682insGGC
NM_005514.6:c.415_416insGGC	NP_005505.2:p.Asp138_Gln139insArg
XM_011514556.1:c.448_449insGGC	XP_011512858.1:p.Asp149_Gln150insArg
XM_011514557.1:c.415_416insGGC	XP_011512859.1:p.Asp138_Gln139insArg
XR_926175.1:n.425_426insGGC
NM_005514.7:c.415_416insGGC	NP_005505.2:p.Asp138_Gln139insArg
NM_005514.8:c.415_416insGGC MANE Select	NP_005505.2:p.Asp138_Gln139insArg