Canonical Allele Identifier: CA823880935
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1554211792

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356477_31356478insACCCC , CM000668.2:g.31356477_31356478insACCCC GRCh38
NC_000006.11:g.31324254_31324255insACCCC , CM000668.1:g.31324254_31324255insACCCC GRCh37
NC_000006.10:g.31432233_31432234insACCCC NCBI36
NG_023187.1:g.5735_5736insGGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-36_1817-35insGGGGT
ENST00000481849.6:n.1817-36_1817-35insGGGGT
ENST00000497377.6:n.1817-36_1817-35insGGGGT
ENST00000640094.2:c.344-36_344-35insGGGGT ENSP00000491275.2:n.344-36_344-35insGGGGT
ENST00000696558.1:c.344-36_344-35insGGGGT ENSP00000512716.1:n.344-36_344-35insGGGGT
ENST00000696559.1:c.344-36_344-35insGGGGT ENSP00000512717.1:n.344-36_344-35insGGGGT
ENST00000696560.1:c.344-36_344-35insGGGGT ENSP00000512718.1:n.344-36_344-35insGGGGT
ENST00000696561.1:c.344-36_344-35insGGGGT ENSP00000512719.1:n.344-36_344-35insGGGGT
ENST00000696562.1:c.344-36_344-35insGGGGT ENSP00000512720.1:n.344-36_344-35insGGGGT
ENST00000412585.7:c.344-36_344-35insGGGGT MANE Select ENSP00000399168.2:n.344-36_344-35insGGGGT
ENST00000412585.6:c.344-36_344-35insGGGGT ENSP00000399168.2:n.344-36_344-35insGGGGT
ENST00000434333.1:c.377-36_377-35insGGGGT ENSP00000405931.1:n.377-36_377-35insGGGGT
ENST00000474381.1:n.219-36_219-35insGGGGT
ENST00000498007.1:n.574_575insGGGGT
NM_005514.6:c.344-36_344-35insGGGGT NP_005505.2:n.344-36_344-35insGGGGT
XM_011514556.1:c.377-36_377-35insGGGGT XP_011512858.1:n.377-36_377-35insGGGGT
XM_011514557.1:c.344-36_344-35insGGGGT XP_011512859.1:n.344-36_344-35insGGGGT
XR_926175.1:n.354-36_354-35insGGGGT
NM_005514.7:c.344-36_344-35insGGGGT NP_005505.2:n.344-36_344-35insGGGGT
NM_005514.8:c.344-36_344-35insGGGGT MANE Select NP_005505.2:n.344-36_344-35insGGGGT