Canonical Allele Identifier: CA3711299

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs773607091
• ExAC: 6:31323036 T / TCAGCCCTGACCTG
• gnomAD v2: 6-31323036-T-TCAGCCCTGACCTG
• gnomAD v3: 6-31355259-T-TCAGCCCTGACCTG
• gnomAD v4: 6-31355259-T-TCAGCCCTGACCTG
• MyVariant Identifiers: chr6:g.31323036_31323037insCAGCCCTGACCTG (hg19) ; chr6:g.31355259_31355260insCAGCCCTGACCTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355259_31355260insCAGCCCTGACCTG , CM000668.2:g.31355259_31355260insCAGCCCTGACCTG	GRCh38
NC_000006.11:g.31323036_31323037insCAGCCCTGACCTG , CM000668.1:g.31323036_31323037insCAGCCCTGACCTG	GRCh37
NC_000006.10:g.31431015_31431016insCAGCCCTGACCTG	NCBI36
NG_023187.1:g.6953_6954insCAGGTCAGGGCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-37_2943-36insCAGGTCAGGGCTG (HLA-B)
ENST00000481849.6:n.2425_2426insCAGGTCAGGGCTG (HLA-B)
ENST00000497377.6:n.2369-37_2369-36insCAGGTCAGGGCTG (HLA-B)
ENST00000640094.2:c.895+57_895+58insCAGGTCAGGGCTG (HLA-B)	ENSP00000491275.2:n.895+57_895+58insCAGGTCAGGGCTG
ENST00000696558.1:c.965-37_965-36insCAGGTCAGGGCTG (HLA-B)	ENSP00000512716.1:n.965-37_965-36insCAGGTCAGGGCTG
ENST00000696559.1:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B)	ENSP00000512717.1:n.896-37_896-36insCAGGTCAGGGCTG
ENST00000696560.1:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B)	ENSP00000512718.1:n.896-37_896-36insCAGGTCAGGGCTG
ENST00000696561.1:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B)	ENSP00000512719.1:n.896-37_896-36insCAGGTCAGGGCTG
ENST00000696562.1:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B)	ENSP00000512720.1:n.896-37_896-36insCAGGTCAGGGCTG
ENST00000412585.7:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B) MANE Select	ENSP00000399168.2:n.896-37_896-36insCAGGTCAGGGCTG
ENST00000640094.1:c.88+57_88+58insCAGGTCAGGGCTG (HLA-B)	ENSP00000491275.1:n.88+57_88+58insCAGGTCAGGGCTG
ENST00000412585.6:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B)	ENSP00000399168.2:n.896-37_896-36insCAGGTCAGGGCTG
ENST00000463574.1:n.487-37_487-36insCAGGTCAGGGCTG (HLA-B)
NM_005514.6:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B)	NP_005505.2:n.896-37_896-36insCAGGTCAGGGCTG
NR_106951.1:n.57_58insCAGGTCAGGGCTG (MIR6891)
XM_011514556.1:c.929-37_929-36insCAGGTCAGGGCTG (HLA-B)	XP_011512858.1:n.929-37_929-36insCAGGTCAGGGCTG
XM_011514557.1:c.895+57_895+58insCAGGTCAGGGCTG (HLA-B)	XP_011512859.1:n.895+57_895+58insCAGGTCAGGGCTG
XR_926175.1:n.1335-37_1335-36insCAGGTCAGGGCTG (HLA-B)
NM_005514.7:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B)	NP_005505.2:n.896-37_896-36insCAGGTCAGGGCTG
NM_005514.8:c.896-37_896-36insCAGGTCAGGGCTG (HLA-B) MANE Select	NP_005505.2:n.896-37_896-36insCAGGTCAGGGCTG