Canonical Allele Identifier: CA1619116334
Gene: HLA-B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31353943_31353944delinsAC , CM000668.2:g.31353943_31353944delinsAC GRCh38
NC_000006.11:g.31321720_31321721delinsAC , CM000668.1:g.31321720_31321721delinsAC GRCh37
NC_000006.10:g.31429699_31429700delinsAC NCBI36
NG_023187.1:g.8269_8270delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3493_3494delinsGT
ENST00000481849.6:n.3453_3454delinsGT
ENST00000497377.6:n.3360_3361delinsGT
ENST00000696558.1:c.1515_1516delinsGT ENSP00000512716.1:n.1515_1516delinsGT
ENST00000696559.1:c.*357_*358delinsGT ENSP00000512717.1:n.*357_*358delinsGT
ENST00000696560.1:c.*357_*358delinsGT ENSP00000512718.1:n.*357_*358delinsGT
ENST00000696561.1:c.*357_*358delinsGT ENSP00000512719.1:n.*357_*358delinsGT
ENST00000696562.1:c.*357_*358delinsGT ENSP00000512720.1:n.*357_*358delinsGT
ENST00000412585.7:c.*357_*358delinsGT MANE Select ENSP00000399168.2:n.*357_*358delinsGT
ENST00000412585.6:c.*357_*358delinsGT ENSP00000399168.2:n.*357_*358delinsGT
ENST00000481849.5:n.681_682delinsGT
ENST00000497377.5:n.845_846delinsGT
NM_005514.6:c.*357_*358delinsGT NP_005505.2:n.*357_*358delinsGT
XM_011514556.1:c.*357_*358delinsGT XP_011512858.1:n.*357_*358delinsGT
XM_011514557.1:c.*357_*358delinsGT XP_011512859.1:n.*357_*358delinsGT
XR_926175.1:n.1885_1886delinsGT
NM_005514.7:c.*357_*358delinsGT NP_005505.2:n.*357_*358delinsGT
NM_005514.8:c.*357_*358delinsGT MANE Select NP_005505.2:n.*357_*358delinsGT
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