Canonical Allele Identifier: CA2677957459
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356557_31356558insT , CM000668.2:g.31356557_31356558insT GRCh38
NC_000006.11:g.31324334_31324335insT , CM000668.1:g.31324334_31324335insT GRCh37
NC_000006.10:g.31432313_31432314insT NCBI36
NG_023187.1:g.5655_5656insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-116_1817-115insA
ENST00000481849.6:n.1817-116_1817-115insA
ENST00000497377.6:n.1817-116_1817-115insA
ENST00000640094.2:c.344-116_344-115insA ENSP00000491275.2:n.344-116_344-115insA
ENST00000696558.1:c.344-116_344-115insA ENSP00000512716.1:n.344-116_344-115insA
ENST00000696559.1:c.344-116_344-115insA ENSP00000512717.1:n.344-116_344-115insA
ENST00000696560.1:c.344-116_344-115insA ENSP00000512718.1:n.344-116_344-115insA
ENST00000696561.1:c.344-116_344-115insA ENSP00000512719.1:n.344-116_344-115insA
ENST00000696562.1:c.344-116_344-115insA ENSP00000512720.1:n.344-116_344-115insA
ENST00000412585.7:c.344-116_344-115insA MANE Select ENSP00000399168.2:n.344-116_344-115insA
ENST00000412585.6:c.344-116_344-115insA ENSP00000399168.2:n.344-116_344-115insA
ENST00000434333.1:c.377-116_377-115insA ENSP00000405931.1:n.377-116_377-115insA
ENST00000474381.1:n.219-116_219-115insA
ENST00000498007.1:n.494_495insA
NM_005514.6:c.344-116_344-115insA NP_005505.2:n.344-116_344-115insA
XM_011514556.1:c.377-116_377-115insA XP_011512858.1:n.377-116_377-115insA
XM_011514557.1:c.344-116_344-115insA XP_011512859.1:n.344-116_344-115insA
XR_926175.1:n.354-116_354-115insA
NM_005514.7:c.344-116_344-115insA NP_005505.2:n.344-116_344-115insA
NM_005514.8:c.344-116_344-115insA MANE Select NP_005505.2:n.344-116_344-115insA