Canonical Allele Identifier: CA2677955890

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355902-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355902_31355903insCC , CM000668.2:g.31355902_31355903insCC	GRCh38
NC_000006.11:g.31323679_31323680insCC , CM000668.1:g.31323679_31323680insCC	GRCh37
NC_000006.10:g.31431658_31431659insCC	NCBI36
NG_023187.1:g.6310_6311insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2356_2357insGG
ENST00000481849.6:n.2092+264_2092+265insGG
ENST00000497377.6:n.2092+264_2092+265insGG
ENST00000640094.2:c.619+264_619+265insGG	ENSP00000491275.2:n.619+264_619+265insGG
ENST00000696558.1:c.620-97_620-96insGG	ENSP00000512716.1:n.620-97_620-96insGG
ENST00000696559.1:c.619+264_619+265insGG	ENSP00000512717.1:n.619+264_619+265insGG
ENST00000696560.1:c.619+264_619+265insGG	ENSP00000512718.1:n.619+264_619+265insGG
ENST00000696561.1:c.619+264_619+265insGG	ENSP00000512719.1:n.619+264_619+265insGG
ENST00000696562.1:c.619+264_619+265insGG	ENSP00000512720.1:n.619+264_619+265insGG
ENST00000412585.7:c.619+264_619+265insGG MANE Select	ENSP00000399168.2:n.619+264_619+265insGG
ENST00000412585.6:c.619+264_619+265insGG	ENSP00000399168.2:n.619+264_619+265insGG
ENST00000434333.1:c.652+264_652+265insGG	ENSP00000405931.1:n.652+264_652+265insGG
ENST00000474381.1:n.758_759insGG
ENST00000498007.1:n.885+264_885+265insGG
NM_005514.6:c.619+264_619+265insGG	NP_005505.2:n.619+264_619+265insGG
XM_011514556.1:c.652+264_652+265insGG	XP_011512858.1:n.652+264_652+265insGG
XM_011514557.1:c.619+264_619+265insGG	XP_011512859.1:n.619+264_619+265insGG
XR_926175.1:n.893_894insGG
NM_005514.7:c.619+264_619+265insGG	NP_005505.2:n.619+264_619+265insGG
NM_005514.8:c.619+264_619+265insGG MANE Select	NP_005505.2:n.619+264_619+265insGG