Canonical Allele Identifier: CA2677957112
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356467_31356468insGGTCCCCCGAGCCCCGCCCC , CM000668.2:g.31356467_31356468insGGTCCCCCGAGCCCCGCCCC GRCh38
NC_000006.11:g.31324244_31324245insGGTCCCCCGAGCCCCGCCCC , CM000668.1:g.31324244_31324245insGGTCCCCCGAGCCCCGCCCC GRCh37
NC_000006.10:g.31432223_31432224insGGTCCCCCGAGCCCCGCCCC NCBI36
NG_023187.1:g.5748_5749insGCGGGGCTCGGGGGACCGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-23_1817-22insGCGGGGCTCGGGGGACCGGG
ENST00000481849.6:n.1817-23_1817-22insGCGGGGCTCGGGGGACCGGG
ENST00000497377.6:n.1817-23_1817-22insGCGGGGCTCGGGGGACCGGG
ENST00000640094.2:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG ENSP00000491275.2:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
ENST00000696558.1:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG ENSP00000512716.1:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
ENST00000696559.1:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG ENSP00000512717.1:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
ENST00000696560.1:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG ENSP00000512718.1:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
ENST00000696561.1:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG ENSP00000512719.1:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
ENST00000696562.1:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG ENSP00000512720.1:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
ENST00000412585.7:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG MANE Select ENSP00000399168.2:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
ENST00000412585.6:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG ENSP00000399168.2:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
ENST00000434333.1:c.377-23_377-22insGCGGGGCTCGGGGGACCGGG ENSP00000405931.1:n.377-23_377-22insGCGGGGCTCGGGGGACCGGG
ENST00000474381.1:n.219-23_219-22insGCGGGGCTCGGGGGACCGGG
ENST00000498007.1:n.587_588insGCGGGGCTCGGGGGACCGGG
NM_005514.6:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG NP_005505.2:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
XM_011514556.1:c.377-23_377-22insGCGGGGCTCGGGGGACCGGG XP_011512858.1:n.377-23_377-22insGCGGGGCTCGGGGGACCGGG
XM_011514557.1:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG XP_011512859.1:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
XR_926175.1:n.354-23_354-22insGCGGGGCTCGGGGGACCGGG
NM_005514.7:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG NP_005505.2:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG
NM_005514.8:c.344-23_344-22insGCGGGGCTCGGGGGACCGGG MANE Select NP_005505.2:n.344-23_344-22insGCGGGGCTCGGGGGACCGGG