Canonical Allele Identifier: CA2677956131

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355999-T-TGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355999_31356000insGGC , CM000668.2:g.31355999_31356000insGGC	GRCh38
NC_000006.11:g.31323776_31323777insGGC , CM000668.1:g.31323776_31323777insGGC	GRCh37
NC_000006.10:g.31431755_31431756insGGC	NCBI36
NG_023187.1:g.6213_6214insGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2259_2260insGCC
ENST00000481849.6:n.2092+167_2092+168insGCC
ENST00000497377.6:n.2092+167_2092+168insGCC
ENST00000640094.2:c.619+167_619+168insGCC	ENSP00000491275.2:n.619+167_619+168insGCC
ENST00000696558.1:c.619+167_619+168insGCC	ENSP00000512716.1:n.619+167_619+168insGCC
ENST00000696559.1:c.619+167_619+168insGCC	ENSP00000512717.1:n.619+167_619+168insGCC
ENST00000696560.1:c.619+167_619+168insGCC	ENSP00000512718.1:n.619+167_619+168insGCC
ENST00000696561.1:c.619+167_619+168insGCC	ENSP00000512719.1:n.619+167_619+168insGCC
ENST00000696562.1:c.619+167_619+168insGCC	ENSP00000512720.1:n.619+167_619+168insGCC
ENST00000412585.7:c.619+167_619+168insGCC MANE Select	ENSP00000399168.2:n.619+167_619+168insGCC
ENST00000412585.6:c.619+167_619+168insGCC	ENSP00000399168.2:n.619+167_619+168insGCC
ENST00000434333.1:c.652+167_652+168insGCC	ENSP00000405931.1:n.652+167_652+168insGCC
ENST00000474381.1:n.661_662insGCC
ENST00000498007.1:n.885+167_885+168insGCC
NM_005514.6:c.619+167_619+168insGCC	NP_005505.2:n.619+167_619+168insGCC
XM_011514556.1:c.652+167_652+168insGCC	XP_011512858.1:n.652+167_652+168insGCC
XM_011514557.1:c.619+167_619+168insGCC	XP_011512859.1:n.619+167_619+168insGCC
XR_926175.1:n.796_797insGCC
NM_005514.7:c.619+167_619+168insGCC	NP_005505.2:n.619+167_619+168insGCC
NM_005514.8:c.619+167_619+168insGCC MANE Select	NP_005505.2:n.619+167_619+168insGCC