Canonical Allele Identifier: CA3711814
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs145974360
gnomAD v2: 6-31324582-T-C
gnomAD v3: 6-31356805-T-C
gnomAD v4: 6-31356805-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356805T>C , CM000668.2:g.31356805T>C GRCh38
NC_000006.11:g.31324582T>C , CM000668.1:g.31324582T>C GRCh37
NC_000006.10:g.31432561T>C NCBI36
NG_023187.1:g.5408A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1699A>G
ENST00000481849.6:n.1699A>G
ENST00000497377.6:n.1699A>G
ENST00000640094.2:c.226A>G ENSP00000491275.2:p.Ile76Val
ENST00000696558.1:c.226A>G ENSP00000512716.1:p.Ile76Val
ENST00000696559.1:c.226A>G ENSP00000512717.1:p.Ile76Val
ENST00000696560.1:c.226A>G ENSP00000512718.1:p.Ile76Val
ENST00000696561.1:c.226A>G ENSP00000512719.1:p.Ile76Val
ENST00000696562.1:c.226A>G ENSP00000512720.1:p.Ile76Val
ENST00000412585.7:c.226A>G MANE Select ENSP00000399168.2:p.Ile76Val
ENST00000412585.6:c.226A>G ENSP00000399168.2:p.Ile76Val
ENST00000434333.1:c.259A>G ENSP00000405931.1:p.Ile87Val
ENST00000474381.1:n.101A>G
ENST00000498007.1:n.247A>G
ENST00000603274.1:n.159T>C
NM_005514.6:c.226A>G NP_005505.2:p.Ile76Val
XM_011514556.1:c.259A>G XP_011512858.1:p.Ile87Val
XM_011514557.1:c.226A>G XP_011512859.1:p.Ile76Val
XR_926175.1:n.236A>G
NM_005514.7:c.226A>G NP_005505.2:p.Ile76Val
NM_005514.8:c.226A>G MANE Select NP_005505.2:p.Ile76Val