Canonical Allele Identifier: CA136836742
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs45560938
gnomAD v3: 6-31357084-A-C
gnomAD v4: 6-31357084-A-C
MyVariant Identifiers: chr6:g.31324861A>C (hg19) chr6:g.31357084A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357084A>C , CM000668.2:g.31357084A>C GRCh38
NC_000006.11:g.31324861A>C , CM000668.1:g.31324861A>C GRCh37
NC_000006.10:g.31432840A>C NCBI36
NG_023187.1:g.5129T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1546+2T>G
ENST00000481849.6:n.1546+2T>G
ENST00000497377.6:n.1546+2T>G
ENST00000640094.2:c.73+2T>G ENSP00000491275.2:n.73+2T>G
ENST00000696558.1:c.73+2T>G ENSP00000512716.1:n.73+2T>G
ENST00000696559.1:c.73+2T>G ENSP00000512717.1:n.73+2T>G
ENST00000696560.1:c.73+2T>G ENSP00000512718.1:n.73+2T>G
ENST00000696561.1:c.73+2T>G ENSP00000512719.1:n.73+2T>G
ENST00000696562.1:c.73+2T>G ENSP00000512720.1:n.73+2T>G
ENST00000412585.7:c.73+2T>G MANE Select ENSP00000399168.2:n.73+2T>G
ENST00000412585.6:c.73+2T>G ENSP00000399168.2:n.73+2T>G
ENST00000434333.1:c.-21T>G ENSP00000405931.1:n.-21T>G
ENST00000498007.1:n.94+2T>G
ENST00000603274.1:n.438A>C
NM_005514.6:c.73+2T>G NP_005505.2:n.73+2T>G
XM_011514557.1:c.73+2T>G XP_011512859.1:n.73+2T>G
XR_926175.1:n.83+2T>G
NM_005514.7:c.73+2T>G NP_005505.2:n.73+2T>G
NM_005514.8:c.73+2T>G MANE Select NP_005505.2:n.73+2T>G
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