Canonical Allele Identifier: CA1619118443
Gene: HLA-B HGNC NCBI
MIR6891 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355242A= , CM000668.2:g.31355242A= GRCh38
NC_000006.11:g.31323019A= , CM000668.1:g.31323019A= GRCh37
NC_000006.10:g.31430998A= NCBI36
NG_023187.1:g.6971T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2943-19T= (HLA-B)
ENST00000481849.6:n.2443T= (HLA-B)
ENST00000497377.6:n.2369-19T= (HLA-B)
ENST00000640094.2:c.895+75T= (HLA-B) ENSP00000491275.2:n.895+75T=
ENST00000696558.1:c.965-19T= (HLA-B) ENSP00000512716.1:n.965-19T=
ENST00000696559.1:c.896-19T= (HLA-B) ENSP00000512717.1:n.896-19T=
ENST00000696560.1:c.896-19T= (HLA-B) ENSP00000512718.1:n.896-19T=
ENST00000696561.1:c.896-19T= (HLA-B) ENSP00000512719.1:n.896-19T=
ENST00000696562.1:c.896-19T= (HLA-B) ENSP00000512720.1:n.896-19T=
ENST00000412585.7:c.896-19T= (HLA-B) MANE Select ENSP00000399168.2:n.896-19T=
ENST00000640094.1:c.88+75T= (HLA-B) ENSP00000491275.1:n.88+75T=
ENST00000412585.6:c.896-19T= (HLA-B) ENSP00000399168.2:n.896-19T=
ENST00000463574.1:n.487-19T= (HLA-B)
NM_005514.6:c.896-19T= (HLA-B) NP_005505.2:n.896-19T=
NR_106951.1:n.75T= (MIR6891)
XM_011514556.1:c.929-19T= (HLA-B) XP_011512858.1:n.929-19T=
XM_011514557.1:c.895+75T= (HLA-B) XP_011512859.1:n.895+75T=
XR_926175.1:n.1335-19T= (HLA-B)
NM_005514.7:c.896-19T= (HLA-B) NP_005505.2:n.896-19T=
NM_005514.8:c.896-19T= (HLA-B) MANE Select NP_005505.2:n.896-19T=