Canonical Allele Identifier: CA3711313

Gene: HLA-B MIR6891

Linked Data

• dbSNP Id: rs756120067
• ExAC: 6:31323059 TG / T
• gnomAD v2: 6-31323059-TG-T
• gnomAD v3: 6-31355282-TG-T
• gnomAD v4: 6-31355282-TG-T
• MyVariant Identifiers: chr6:g.31323060del (hg19) ; chr6:g.31323060_31323064delinsAGAA (hg19) ; chr6:g.31355283del (hg38) ; chr6:g.31355283_31355287delinsAGAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355283del , CM000668.2:g.31355283del	GRCh38
NC_000006.11:g.31323060del , CM000668.1:g.31323060del	GRCh37
NC_000006.10:g.31431039del	NCBI36
NG_023187.1:g.6930del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2942+34del (HLA-B)
ENST00000481849.6:n.2402del (HLA-B)
ENST00000497377.6:n.2368+34del (HLA-B)
ENST00000640094.2:c.895+34del (HLA-B)	ENSP00000491275.2:n.895+34del
ENST00000696558.1:c.964+34del (HLA-B)	ENSP00000512716.1:n.964+34del
ENST00000696559.1:c.895+34del (HLA-B)	ENSP00000512717.1:n.895+34del
ENST00000696560.1:c.895+34del (HLA-B)	ENSP00000512718.1:n.895+34del
ENST00000696561.1:c.895+34del (HLA-B)	ENSP00000512719.1:n.895+34del
ENST00000696562.1:c.895+34del (HLA-B)	ENSP00000512720.1:n.895+34del
ENST00000412585.7:c.895+34del (HLA-B) MANE Select	ENSP00000399168.2:n.895+34del
ENST00000640094.1:c.88+34del (HLA-B)	ENSP00000491275.1:n.88+34del
ENST00000412585.6:c.895+34del (HLA-B)	ENSP00000399168.2:n.895+34del
ENST00000463574.1:n.486+34del (HLA-B)
NM_005514.6:c.895+34del (HLA-B)	NP_005505.2:n.895+34del
NR_106951.1:n.34del (MIR6891)
XM_011514556.1:c.928+34del (HLA-B)	XP_011512858.1:n.928+34del
XM_011514557.1:c.895+34del (HLA-B)	XP_011512859.1:n.895+34del
XR_926175.1:n.1334+34del (HLA-B)
NM_005514.7:c.895+34del (HLA-B)	NP_005505.2:n.895+34del
NM_005514.8:c.895+34del (HLA-B) MANE Select	NP_005505.2:n.895+34del