Canonical Allele Identifier: CA136833529
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341333
gnomAD v4: 6-31356180-C-G
MyVariant Identifiers: chr6:g.31323957C>G (hg19) chr6:g.31356180C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356180C>G , CM000668.2:g.31356180C>G GRCh38
NC_000006.11:g.31323957C>G , CM000668.1:g.31323957C>G GRCh37
NC_000006.10:g.31431936C>G NCBI36
NG_023187.1:g.6033G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2079G>C
ENST00000481849.6:n.2079G>C
ENST00000497377.6:n.2079G>C
ENST00000640094.2:c.606G>C ENSP00000491275.2:p.Lys202Asn
ENST00000696558.1:c.606G>C ENSP00000512716.1:p.Lys202Asn
ENST00000696559.1:c.606G>C ENSP00000512717.1:p.Lys202Asn
ENST00000696560.1:c.606G>C ENSP00000512718.1:p.Lys202Asn
ENST00000696561.1:c.606G>C ENSP00000512719.1:p.Lys202Asn
ENST00000696562.1:c.606G>C ENSP00000512720.1:p.Lys202Asn
ENST00000412585.7:c.606G>C MANE Select ENSP00000399168.2:p.Lys202Asn
ENST00000412585.6:c.606G>C ENSP00000399168.2:p.Lys202Asn
ENST00000434333.1:c.639G>C ENSP00000405931.1:p.Lys213Asn
ENST00000474381.1:n.481G>C
ENST00000498007.1:n.872G>C
NM_005514.6:c.606G>C NP_005505.2:p.Lys202Asn
XM_011514556.1:c.639G>C XP_011512858.1:p.Lys213Asn
XM_011514557.1:c.606G>C XP_011512859.1:p.Lys202Asn
XR_926175.1:n.616G>C
NM_005514.7:c.606G>C NP_005505.2:p.Lys202Asn
NM_005514.8:c.606G>C MANE Select NP_005505.2:p.Lys202Asn
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