Canonical Allele Identifier: CA1619118485

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs1766824054

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355258_31355259insCCAAGCCTCAGCCCTGACCT , CM000668.2:g.31355258_31355259insCCAAGCCTCAGCCCTGACCT	GRCh38
NC_000006.11:g.31323035_31323036insCCAAGCCTCAGCCCTGACCT , CM000668.1:g.31323035_31323036insCCAAGCCTCAGCCCTGACCT	GRCh37
NC_000006.10:g.31431014_31431015insCCAAGCCTCAGCCCTGACCT	NCBI36
NG_023187.1:g.6954_6955insAGGTCAGGGCTGAGGCTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-36_2943-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)
ENST00000481849.6:n.2426_2427insAGGTCAGGGCTGAGGCTTGG (HLA-B)
ENST00000497377.6:n.2369-36_2369-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)
ENST00000640094.2:c.895+58_895+59insAGGTCAGGGCTGAGGCTTGG (HLA-B)	ENSP00000491275.2:n.895+58_895+59insAGGTCAGGGCTGAGGCTTGG
ENST00000696558.1:c.965-36_965-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	ENSP00000512716.1:n.965-36_965-35insAGGTCAGGGCTGAGGCTTGG
ENST00000696559.1:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	ENSP00000512717.1:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG
ENST00000696560.1:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	ENSP00000512718.1:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG
ENST00000696561.1:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	ENSP00000512719.1:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG
ENST00000696562.1:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	ENSP00000512720.1:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG
ENST00000412585.7:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B) MANE Select	ENSP00000399168.2:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG
ENST00000640094.1:c.88+58_88+59insAGGTCAGGGCTGAGGCTTGG (HLA-B)	ENSP00000491275.1:n.88+58_88+59insAGGTCAGGGCTGAGGCTTGG
ENST00000412585.6:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	ENSP00000399168.2:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG
ENST00000463574.1:n.487-36_487-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)
NM_005514.6:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	NP_005505.2:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG
NR_106951.1:n.58_59insAGGTCAGGGCTGAGGCTTGG (MIR6891)
XM_011514556.1:c.929-36_929-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	XP_011512858.1:n.929-36_929-35insAGGTCAGGGCTGAGGCTTGG
XM_011514557.1:c.895+58_895+59insAGGTCAGGGCTGAGGCTTGG (HLA-B)	XP_011512859.1:n.895+58_895+59insAGGTCAGGGCTGAGGCTTGG
XR_926175.1:n.1335-36_1335-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)
NM_005514.7:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B)	NP_005505.2:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG
NM_005514.8:c.896-36_896-35insAGGTCAGGGCTGAGGCTTGG (HLA-B) MANE Select	NP_005505.2:n.896-36_896-35insAGGTCAGGGCTGAGGCTTGG