Canonical Allele Identifier: CA136836325
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341206
gnomAD v3: 6-31356699-T-C
gnomAD v4: 6-31356699-T-C
MyVariant Identifiers: chr6:g.31324476T>C (hg19) chr6:g.31356699T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356699T>C , CM000668.2:g.31356699T>C GRCh38
NC_000006.11:g.31324476T>C , CM000668.1:g.31324476T>C GRCh37
NC_000006.10:g.31432455T>C NCBI36
NG_023187.1:g.5514A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1805A>G
ENST00000481849.6:n.1805A>G
ENST00000497377.6:n.1805A>G
ENST00000640094.2:c.332A>G ENSP00000491275.2:p.Gln111Arg
ENST00000696558.1:c.332A>G ENSP00000512716.1:p.Gln111Arg
ENST00000696559.1:c.332A>G ENSP00000512717.1:p.Gln111Arg
ENST00000696560.1:c.332A>G ENSP00000512718.1:p.Gln111Arg
ENST00000696561.1:c.332A>G ENSP00000512719.1:p.Gln111Arg
ENST00000696562.1:c.332A>G ENSP00000512720.1:p.Gln111Arg
ENST00000412585.7:c.332A>G MANE Select ENSP00000399168.2:p.Gln111Arg
ENST00000412585.6:c.332A>G ENSP00000399168.2:p.Gln111Arg
ENST00000434333.1:c.365A>G ENSP00000405931.1:p.Gln122Arg
ENST00000474381.1:n.207A>G
ENST00000498007.1:n.353A>G
ENST00000603274.1:n.53T>C
NM_005514.6:c.332A>G NP_005505.2:p.Gln111Arg
XM_011514556.1:c.365A>G XP_011512858.1:p.Gln122Arg
XM_011514557.1:c.332A>G XP_011512859.1:p.Gln111Arg
XR_926175.1:n.342A>G
NM_005514.7:c.332A>G NP_005505.2:p.Gln111Arg
NM_005514.8:c.332A>G MANE Select NP_005505.2:p.Gln111Arg
Search 100 bp 5'
Search 100 bp 3'