Canonical Allele Identifier: CA566689213

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31324262-C-CCCAGT
• MyVariant Identifiers: chr6:g.31324262_31324263insCCAGT (hg19) ; chr6:g.31356485_31356486insCCAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356487_31356488insAGTCC , CM000668.2:g.31356487_31356488insAGTCC	GRCh38
NC_000006.11:g.31324264_31324265insAGTCC , CM000668.1:g.31324264_31324265insAGTCC	GRCh37
NC_000006.10:g.31432243_31432244insAGTCC	NCBI36
NG_023187.1:g.5727_5728insACTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1817-44_1817-43insACTGG
ENST00000481849.6:n.1817-44_1817-43insACTGG
ENST00000497377.6:n.1817-44_1817-43insACTGG
ENST00000640094.2:c.344-44_344-43insACTGG	ENSP00000491275.2:n.344-44_344-43insACTGG
ENST00000696558.1:c.344-44_344-43insACTGG	ENSP00000512716.1:n.344-44_344-43insACTGG
ENST00000696559.1:c.344-44_344-43insACTGG	ENSP00000512717.1:n.344-44_344-43insACTGG
ENST00000696560.1:c.344-44_344-43insACTGG	ENSP00000512718.1:n.344-44_344-43insACTGG
ENST00000696561.1:c.344-44_344-43insACTGG	ENSP00000512719.1:n.344-44_344-43insACTGG
ENST00000696562.1:c.344-44_344-43insACTGG	ENSP00000512720.1:n.344-44_344-43insACTGG
ENST00000412585.7:c.344-44_344-43insACTGG MANE Select	ENSP00000399168.2:n.344-44_344-43insACTGG
ENST00000412585.6:c.344-44_344-43insACTGG	ENSP00000399168.2:n.344-44_344-43insACTGG
ENST00000434333.1:c.377-44_377-43insACTGG	ENSP00000405931.1:n.377-44_377-43insACTGG
ENST00000474381.1:n.219-44_219-43insACTGG
ENST00000498007.1:n.566_567insACTGG
NM_005514.6:c.344-44_344-43insACTGG	NP_005505.2:n.344-44_344-43insACTGG
XM_011514556.1:c.377-44_377-43insACTGG	XP_011512858.1:n.377-44_377-43insACTGG
XM_011514557.1:c.344-44_344-43insACTGG	XP_011512859.1:n.344-44_344-43insACTGG
XR_926175.1:n.354-44_354-43insACTGG
NM_005514.7:c.344-44_344-43insACTGG	NP_005505.2:n.344-44_344-43insACTGG
NM_005514.8:c.344-44_344-43insACTGG MANE Select	NP_005505.2:n.344-44_344-43insACTGG