Canonical Allele Identifier: CA566689202

Gene: HLA-B

Linked Data

• dbSNP Id: rs1240941850
• gnomAD v2: 6-31324250-C-CA
• gnomAD v4: 6-31356473-C-CA
• MyVariant Identifiers: chr6:g.31324250_31324251insA (hg19) ; chr6:g.31356473_31356474insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356473_31356474insA , CM000668.2:g.31356473_31356474insA	GRCh38
NC_000006.11:g.31324250_31324251insA , CM000668.1:g.31324250_31324251insA	GRCh37
NC_000006.10:g.31432229_31432230insA	NCBI36
NG_023187.1:g.5739_5740insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1817-32_1817-31insT
ENST00000481849.6:n.1817-32_1817-31insT
ENST00000497377.6:n.1817-32_1817-31insT
ENST00000640094.2:c.344-32_344-31insT	ENSP00000491275.2:n.344-32_344-31insT
ENST00000696558.1:c.344-32_344-31insT	ENSP00000512716.1:n.344-32_344-31insT
ENST00000696559.1:c.344-32_344-31insT	ENSP00000512717.1:n.344-32_344-31insT
ENST00000696560.1:c.344-32_344-31insT	ENSP00000512718.1:n.344-32_344-31insT
ENST00000696561.1:c.344-32_344-31insT	ENSP00000512719.1:n.344-32_344-31insT
ENST00000696562.1:c.344-32_344-31insT	ENSP00000512720.1:n.344-32_344-31insT
ENST00000412585.7:c.344-32_344-31insT MANE Select	ENSP00000399168.2:n.344-32_344-31insT
ENST00000412585.6:c.344-32_344-31insT	ENSP00000399168.2:n.344-32_344-31insT
ENST00000434333.1:c.377-32_377-31insT	ENSP00000405931.1:n.377-32_377-31insT
ENST00000474381.1:n.219-32_219-31insT
ENST00000498007.1:n.578_579insT
NM_005514.6:c.344-32_344-31insT	NP_005505.2:n.344-32_344-31insT
XM_011514556.1:c.377-32_377-31insT	XP_011512858.1:n.377-32_377-31insT
XM_011514557.1:c.344-32_344-31insT	XP_011512859.1:n.344-32_344-31insT
XR_926175.1:n.354-32_354-31insT
NM_005514.7:c.344-32_344-31insT	NP_005505.2:n.344-32_344-31insT
NM_005514.8:c.344-32_344-31insT MANE Select	NP_005505.2:n.344-32_344-31insT