Canonical Allele Identifier: CA136836722
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs796503852

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356965_31356966delinsCC , CM000668.2:g.31356965_31356966delinsCC GRCh38
NC_000006.11:g.31324742_31324743delinsCC , CM000668.1:g.31324742_31324743delinsCC GRCh37
NC_000006.10:g.31432721_31432722delinsCC NCBI36
NG_023187.1:g.5247_5248delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1547-9_1547-8delinsGG
ENST00000481849.6:n.1547-9_1547-8delinsGG
ENST00000497377.6:n.1547-9_1547-8delinsGG
ENST00000640094.2:c.74-9_74-8delinsGG ENSP00000491275.2:n.74-9_74-8delinsGG
ENST00000696558.1:c.74-9_74-8delinsGG ENSP00000512716.1:n.74-9_74-8delinsGG
ENST00000696559.1:c.74-9_74-8delinsGG ENSP00000512717.1:n.74-9_74-8delinsGG
ENST00000696560.1:c.74-9_74-8delinsGG ENSP00000512718.1:n.74-9_74-8delinsGG
ENST00000696561.1:c.74-9_74-8delinsGG ENSP00000512719.1:n.74-9_74-8delinsGG
ENST00000696562.1:c.74-9_74-8delinsGG ENSP00000512720.1:n.74-9_74-8delinsGG
ENST00000412585.7:c.74-9_74-8delinsGG MANE Select ENSP00000399168.2:n.74-9_74-8delinsGG
ENST00000412585.6:c.74-9_74-8delinsGG ENSP00000399168.2:n.74-9_74-8delinsGG
ENST00000434333.1:c.98_99delinsGG ENSP00000405931.1:p.Ser33Trp
ENST00000498007.1:n.95-9_95-8delinsGG
ENST00000603274.1:n.319_320delinsCC
NM_005514.6:c.74-9_74-8delinsGG NP_005505.2:n.74-9_74-8delinsGG
XM_011514556.1:c.98_99delinsGG XP_011512858.1:p.Ser33Trp
XM_011514557.1:c.74-9_74-8delinsGG XP_011512859.1:n.74-9_74-8delinsGG
XR_926175.1:n.84-9_84-8delinsGG
NM_005514.7:c.74-9_74-8delinsGG NP_005505.2:n.74-9_74-8delinsGG
NM_005514.8:c.74-9_74-8delinsGG MANE Select NP_005505.2:n.74-9_74-8delinsGG