Canonical Allele Identifier: CA3711195

Gene: HLA-B

Linked Data

• dbSNP Id: rs757165948
• ExAC: 6:31322359 A / AGGAATTATG
• gnomAD v2: 6-31322359-A-AGGAATTATG
• gnomAD v3: 6-31354582-A-AGGAATTATG
• gnomAD v4: 6-31354582-A-AGGAATTATG
• MyVariant Identifiers: chr6:g.31322359_31322360insGGAATTATG (hg19) ; chr6:g.31354582_31354583insGGAATTATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354585_31354593dup , CM000668.2:g.31354585_31354593dup	GRCh38
NC_000006.11:g.31322362_31322370dup , CM000668.1:g.31322362_31322370dup	GRCh37
NC_000006.10:g.31430341_31430349dup	NCBI36
NG_023187.1:g.7622_7630dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3092+42_3092+50dup
ENST00000481849.6:n.3052+42_3052+50dup
ENST00000497377.6:n.2959+42_2959+50dup
ENST00000640094.2:c.928+42_928+50dup	ENSP00000491275.2:n.928+42_928+50dup
ENST00000696558.1:c.1114+42_1114+50dup	ENSP00000512716.1:n.1114+42_1114+50dup
ENST00000696559.1:c.1045+42_1045+50dup	ENSP00000512717.1:n.1045+42_1045+50dup
ENST00000696560.1:c.1045+42_1045+50dup	ENSP00000512718.1:n.1045+42_1045+50dup
ENST00000696561.1:c.1045+42_1045+50dup	ENSP00000512719.1:n.1045+42_1045+50dup
ENST00000696562.1:c.1045+42_1045+50dup	ENSP00000512720.1:n.1045+42_1045+50dup
ENST00000412585.7:c.1045+42_1045+50dup MANE Select	ENSP00000399168.2:n.1045+42_1045+50dup
ENST00000640094.1:c.121+42_121+50dup	ENSP00000491275.1:n.121+42_121+50dup
ENST00000412585.6:c.1045+42_1045+50dup	ENSP00000399168.2:n.1045+42_1045+50dup
ENST00000481849.5:n.216_224dup
ENST00000497377.5:n.444+42_444+50dup
NM_005514.6:c.1045+42_1045+50dup	NP_005505.2:n.1045+42_1045+50dup
XM_011514556.1:c.1078+42_1078+50dup	XP_011512858.1:n.1078+42_1078+50dup
XM_011514557.1:c.928+42_928+50dup	XP_011512859.1:n.928+42_928+50dup
XR_926175.1:n.1484+42_1484+50dup
NM_005514.7:c.1045+42_1045+50dup	NP_005505.2:n.1045+42_1045+50dup
NM_005514.8:c.1045+42_1045+50dup MANE Select	NP_005505.2:n.1045+42_1045+50dup