Canonical Allele Identifier: CA1087464853
Gene: HLA-B HGNC NCBI
MIR6891 HGNC NCBI

Linked Data

dbSNP Id: rs375780719
gnomAD v3: 6-31355226-G-C
gnomAD v4: 6-31355226-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355226G>C , CM000668.2:g.31355226G>C GRCh38
NC_000006.11:g.31323003G>C , CM000668.1:g.31323003G>C GRCh37
NC_000006.10:g.31430982G>C NCBI36
NG_023187.1:g.6987C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2943-3C>G (HLA-B)
ENST00000481849.6:n.2459C>G (HLA-B)
ENST00000497377.6:n.2369-3C>G (HLA-B)
ENST00000640094.2:c.895+91C>G (HLA-B) ENSP00000491275.2:n.895+91C>G
ENST00000696558.1:c.965-3C>G (HLA-B) ENSP00000512716.1:n.965-3C>G
ENST00000696559.1:c.896-3C>G (HLA-B) ENSP00000512717.1:n.896-3C>G
ENST00000696560.1:c.896-3C>G (HLA-B) ENSP00000512718.1:n.896-3C>G
ENST00000696561.1:c.896-3C>G (HLA-B) ENSP00000512719.1:n.896-3C>G
ENST00000696562.1:c.896-3C>G (HLA-B) ENSP00000512720.1:n.896-3C>G
ENST00000412585.7:c.896-3C>G (HLA-B) MANE Select ENSP00000399168.2:n.896-3C>G
ENST00000640094.1:c.88+91C>G (HLA-B) ENSP00000491275.1:n.88+91C>G
ENST00000412585.6:c.896-3C>G (HLA-B) ENSP00000399168.2:n.896-3C>G
ENST00000463574.1:n.487-3C>G (HLA-B)
NM_005514.6:c.896-3C>G (HLA-B) NP_005505.2:n.896-3C>G
NR_106951.1:n.91C>G (MIR6891)
XM_011514556.1:c.929-3C>G (HLA-B) XP_011512858.1:n.929-3C>G
XM_011514557.1:c.895+91C>G (HLA-B) XP_011512859.1:n.895+91C>G
XR_926175.1:n.1335-3C>G (HLA-B)
NM_005514.7:c.896-3C>G (HLA-B) NP_005505.2:n.896-3C>G
NM_005514.8:c.896-3C>G (HLA-B) MANE Select NP_005505.2:n.896-3C>G
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