Canonical Allele Identifier: CA136836634
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs76827460
gnomAD v4: 6-31356868-T-C
MyVariant Identifiers: chr6:g.31324645T>C (hg19) chr6:g.31356868T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356868T>C , CM000668.2:g.31356868T>C GRCh38
NC_000006.11:g.31324645T>C , CM000668.1:g.31324645T>C GRCh37
NC_000006.10:g.31432624T>C NCBI36
NG_023187.1:g.5345A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1636A>G
ENST00000481849.6:n.1636A>G
ENST00000497377.6:n.1636A>G
ENST00000640094.2:c.163A>G ENSP00000491275.2:p.Thr55Ala
ENST00000696558.1:c.163A>G ENSP00000512716.1:p.Thr55Ala
ENST00000696559.1:c.163A>G ENSP00000512717.1:p.Thr55Ala
ENST00000696560.1:c.163A>G ENSP00000512718.1:p.Thr55Ala
ENST00000696561.1:c.163A>G ENSP00000512719.1:p.Thr55Ala
ENST00000696562.1:c.163A>G ENSP00000512720.1:p.Thr55Ala
ENST00000412585.7:c.163A>G MANE Select ENSP00000399168.2:p.Thr55Ala
ENST00000412585.6:c.163A>G ENSP00000399168.2:p.Thr55Ala
ENST00000434333.1:c.196A>G ENSP00000405931.1:p.Thr66Ala
ENST00000474381.1:n.38A>G
ENST00000498007.1:n.184A>G
ENST00000603274.1:n.222T>C
NM_005514.6:c.163A>G NP_005505.2:p.Thr55Ala
XM_011514556.1:c.196A>G XP_011512858.1:p.Thr66Ala
XM_011514557.1:c.163A>G XP_011512859.1:p.Thr55Ala
XR_926175.1:n.173A>G
NM_005514.7:c.163A>G NP_005505.2:p.Thr55Ala
NM_005514.8:c.163A>G MANE Select NP_005505.2:p.Thr55Ala
Search 100 bp 5'
Search 100 bp 3'