Canonical Allele Identifier: CA566689264

Gene: HLA-B

Linked Data

• dbSNP Id: rs1460090072
• gnomAD v2: 6-31323959-T-TCCC
• MyVariant Identifiers: chr6:g.31323959_31323960insCCC (hg19) ; chr6:g.31356182_31356183insCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356182_31356183insCCC , CM000668.2:g.31356182_31356183insCCC	GRCh38
NC_000006.11:g.31323959_31323960insCCC , CM000668.1:g.31323959_31323960insCCC	GRCh37
NC_000006.10:g.31431938_31431939insCCC	NCBI36
NG_023187.1:g.6030_6031insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2076_2077insGGG
ENST00000481849.6:n.2076_2077insGGG
ENST00000497377.6:n.2076_2077insGGG
ENST00000640094.2:c.603_604insGGG	ENSP00000491275.2:p.Asp201_Lys202insGly
ENST00000696558.1:c.603_604insGGG	ENSP00000512716.1:p.Asp201_Lys202insGly
ENST00000696559.1:c.603_604insGGG	ENSP00000512717.1:p.Asp201_Lys202insGly
ENST00000696560.1:c.603_604insGGG	ENSP00000512718.1:p.Asp201_Lys202insGly
ENST00000696561.1:c.603_604insGGG	ENSP00000512719.1:p.Asp201_Lys202insGly
ENST00000696562.1:c.603_604insGGG	ENSP00000512720.1:p.Asp201_Lys202insGly
ENST00000412585.7:c.603_604insGGG MANE Select	ENSP00000399168.2:p.Asp201_Lys202insGly
ENST00000412585.6:c.603_604insGGG	ENSP00000399168.2:p.Asp201_Lys202insGly
ENST00000434333.1:c.636_637insGGG	ENSP00000405931.1:p.Asp212_Lys213insGly
ENST00000474381.1:n.478_479insGGG
ENST00000498007.1:n.869_870insGGG
NM_005514.6:c.603_604insGGG	NP_005505.2:p.Asp201_Lys202insGly
XM_011514556.1:c.636_637insGGG	XP_011512858.1:p.Asp212_Lys213insGly
XM_011514557.1:c.603_604insGGG	XP_011512859.1:p.Asp201_Lys202insGly
XR_926175.1:n.613_614insGGG
NM_005514.7:c.603_604insGGG	NP_005505.2:p.Asp201_Lys202insGly
NM_005514.8:c.603_604insGGG MANE Select	NP_005505.2:p.Asp201_Lys202insGly