Canonical Allele Identifier: CA1619118463

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs1766820360

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355253_31355256dup , CM000668.2:g.31355253_31355256dup	GRCh38
NC_000006.11:g.31323030_31323033dup , CM000668.1:g.31323030_31323033dup	GRCh37
NC_000006.10:g.31431009_31431012dup	NCBI36
NG_023187.1:g.6958_6961dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-32_2943-29dup (HLA-B)
ENST00000481849.6:n.2430_2433dup (HLA-B)
ENST00000497377.6:n.2369-32_2369-29dup (HLA-B)
ENST00000640094.2:c.895+62_895+65dup (HLA-B)	ENSP00000491275.2:n.895+62_895+65dup
ENST00000696558.1:c.965-32_965-29dup (HLA-B)	ENSP00000512716.1:n.965-32_965-29dup
ENST00000696559.1:c.896-32_896-29dup (HLA-B)	ENSP00000512717.1:n.896-32_896-29dup
ENST00000696560.1:c.896-32_896-29dup (HLA-B)	ENSP00000512718.1:n.896-32_896-29dup
ENST00000696561.1:c.896-32_896-29dup (HLA-B)	ENSP00000512719.1:n.896-32_896-29dup
ENST00000696562.1:c.896-32_896-29dup (HLA-B)	ENSP00000512720.1:n.896-32_896-29dup
ENST00000412585.7:c.896-32_896-29dup (HLA-B) MANE Select	ENSP00000399168.2:n.896-32_896-29dup
ENST00000640094.1:c.88+62_88+65dup (HLA-B)	ENSP00000491275.1:n.88+62_88+65dup
ENST00000412585.6:c.896-32_896-29dup (HLA-B)	ENSP00000399168.2:n.896-32_896-29dup
ENST00000463574.1:n.487-32_487-29dup (HLA-B)
NM_005514.6:c.896-32_896-29dup (HLA-B)	NP_005505.2:n.896-32_896-29dup
NR_106951.1:n.62_65dup (MIR6891)
XM_011514556.1:c.929-32_929-29dup (HLA-B)	XP_011512858.1:n.929-32_929-29dup
XM_011514557.1:c.895+62_895+65dup (HLA-B)	XP_011512859.1:n.895+62_895+65dup
XR_926175.1:n.1335-32_1335-29dup (HLA-B)
NM_005514.7:c.896-32_896-29dup (HLA-B)	NP_005505.2:n.896-32_896-29dup
NM_005514.8:c.896-32_896-29dup (HLA-B) MANE Select	NP_005505.2:n.896-32_896-29dup