Canonical Allele Identifier: CA1087464935

Gene: HLA-B MIR6891

Linked Data

• gnomAD v3: 6-31355255-A-C
• gnomAD v4: 6-31355255-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355255A>C , CM000668.2:g.31355255A>C	GRCh38
NC_000006.11:g.31323032A>C , CM000668.1:g.31323032A>C	GRCh37
NC_000006.10:g.31431011A>C	NCBI36
NG_023187.1:g.6958T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2943-32T>G (HLA-B)
ENST00000481849.6:n.2430T>G (HLA-B)
ENST00000497377.6:n.2369-32T>G (HLA-B)
ENST00000640094.2:c.895+62T>G (HLA-B)	ENSP00000491275.2:n.895+62T>G
ENST00000696558.1:c.965-32T>G (HLA-B)	ENSP00000512716.1:n.965-32T>G
ENST00000696559.1:c.896-32T>G (HLA-B)	ENSP00000512717.1:n.896-32T>G
ENST00000696560.1:c.896-32T>G (HLA-B)	ENSP00000512718.1:n.896-32T>G
ENST00000696561.1:c.896-32T>G (HLA-B)	ENSP00000512719.1:n.896-32T>G
ENST00000696562.1:c.896-32T>G (HLA-B)	ENSP00000512720.1:n.896-32T>G
ENST00000412585.7:c.896-32T>G (HLA-B) MANE Select	ENSP00000399168.2:n.896-32T>G
ENST00000640094.1:c.88+62T>G (HLA-B)	ENSP00000491275.1:n.88+62T>G
ENST00000412585.6:c.896-32T>G (HLA-B)	ENSP00000399168.2:n.896-32T>G
ENST00000463574.1:n.487-32T>G (HLA-B)
NM_005514.6:c.896-32T>G (HLA-B)	NP_005505.2:n.896-32T>G
NR_106951.1:n.62T>G (MIR6891)
XM_011514556.1:c.929-32T>G (HLA-B)	XP_011512858.1:n.929-32T>G
XM_011514557.1:c.895+62T>G (HLA-B)	XP_011512859.1:n.895+62T>G
XR_926175.1:n.1335-32T>G (HLA-B)
NM_005514.7:c.896-32T>G (HLA-B)	NP_005505.2:n.896-32T>G
NM_005514.8:c.896-32T>G (HLA-B) MANE Select	NP_005505.2:n.896-32T>G