Canonical Allele Identifier: CA1619113818
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356964_31356965delinsGT , CM000668.2:g.31356964_31356965delinsGT GRCh38
NC_000006.11:g.31324741_31324742delinsGT , CM000668.1:g.31324741_31324742delinsGT GRCh37
NC_000006.10:g.31432720_31432721delinsGT NCBI36
NG_023187.1:g.5248_5249delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1547-8_1547-7delinsAC
ENST00000481849.6:n.1547-8_1547-7delinsAC
ENST00000497377.6:n.1547-8_1547-7delinsAC
ENST00000640094.2:c.74-8_74-7delinsAC ENSP00000491275.2:n.74-8_74-7delinsAC
ENST00000696558.1:c.74-8_74-7delinsAC ENSP00000512716.1:n.74-8_74-7delinsAC
ENST00000696559.1:c.74-8_74-7delinsAC ENSP00000512717.1:n.74-8_74-7delinsAC
ENST00000696560.1:c.74-8_74-7delinsAC ENSP00000512718.1:n.74-8_74-7delinsAC
ENST00000696561.1:c.74-8_74-7delinsAC ENSP00000512719.1:n.74-8_74-7delinsAC
ENST00000696562.1:c.74-8_74-7delinsAC ENSP00000512720.1:n.74-8_74-7delinsAC
ENST00000412585.7:c.74-8_74-7delinsAC MANE Select ENSP00000399168.2:n.74-8_74-7delinsAC
ENST00000412585.6:c.74-8_74-7delinsAC ENSP00000399168.2:n.74-8_74-7delinsAC
ENST00000434333.1:c.99_100delinsAC ENSP00000405931.1:p.Ser33=
ENST00000498007.1:n.95-8_95-7delinsAC
ENST00000603274.1:n.318_319delinsGT
NM_005514.6:c.74-8_74-7delinsAC NP_005505.2:n.74-8_74-7delinsAC
XM_011514556.1:c.99_100delinsAC XP_011512858.1:p.Ser33=
XM_011514557.1:c.74-8_74-7delinsAC XP_011512859.1:n.74-8_74-7delinsAC
XR_926175.1:n.84-8_84-7delinsAC
NM_005514.7:c.74-8_74-7delinsAC NP_005505.2:n.74-8_74-7delinsAC
NM_005514.8:c.74-8_74-7delinsAC MANE Select NP_005505.2:n.74-8_74-7delinsAC