Canonical Allele Identifier: CA2834601269

Gene: HLA-B MIR6891

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355254_31355255del , CM000668.2:g.31355254_31355255del	GRCh38
NC_000006.11:g.31323031_31323032del , CM000668.1:g.31323031_31323032del	GRCh37
NC_000006.10:g.31431010_31431011del	NCBI36
NG_023187.1:g.6958_6959del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2943-32_2943-31del (HLA-B)
ENST00000481849.6:n.2430_2431del (HLA-B)
ENST00000497377.6:n.2369-32_2369-31del (HLA-B)
ENST00000640094.2:c.895+62_895+63del (HLA-B)	ENSP00000491275.2:n.895+62_895+63del
ENST00000696558.1:c.965-32_965-31del (HLA-B)	ENSP00000512716.1:n.965-32_965-31del
ENST00000696559.1:c.896-32_896-31del (HLA-B)	ENSP00000512717.1:n.896-32_896-31del
ENST00000696560.1:c.896-32_896-31del (HLA-B)	ENSP00000512718.1:n.896-32_896-31del
ENST00000696561.1:c.896-32_896-31del (HLA-B)	ENSP00000512719.1:n.896-32_896-31del
ENST00000696562.1:c.896-32_896-31del (HLA-B)	ENSP00000512720.1:n.896-32_896-31del
ENST00000412585.7:c.896-32_896-31del (HLA-B) MANE Select	ENSP00000399168.2:n.896-32_896-31del
ENST00000640094.1:c.88+62_88+63del (HLA-B)	ENSP00000491275.1:n.88+62_88+63del
ENST00000412585.6:c.896-32_896-31del (HLA-B)	ENSP00000399168.2:n.896-32_896-31del
ENST00000463574.1:n.487-32_487-31del (HLA-B)
NM_005514.6:c.896-32_896-31del (HLA-B)	NP_005505.2:n.896-32_896-31del
NR_106951.1:n.62_63del (MIR6891)
XM_011514556.1:c.929-32_929-31del (HLA-B)	XP_011512858.1:n.929-32_929-31del
XM_011514557.1:c.895+62_895+63del (HLA-B)	XP_011512859.1:n.895+62_895+63del
XR_926175.1:n.1335-32_1335-31del (HLA-B)
NM_005514.7:c.896-32_896-31del (HLA-B)	NP_005505.2:n.896-32_896-31del
NM_005514.8:c.896-32_896-31del (HLA-B) MANE Select	NP_005505.2:n.896-32_896-31del