Canonical Allele Identifier: CA2677958085
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357388_31357389insCCA , CM000668.2:g.31357388_31357389insCCA GRCh38
NC_000006.11:g.31325165_31325166insCCA , CM000668.1:g.31325165_31325166insCCA GRCh37
NC_000006.10:g.31433144_31433145insCCA NCBI36
NG_023187.1:g.4824_4825insTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-96_1339-95insTGG
ENST00000481849.6:n.1339-96_1339-95insTGG
ENST00000497377.6:n.1339-96_1339-95insTGG
ENST00000696559.1:c.-135-96_-135-95insTGG ENSP00000512717.1:n.-135-96_-135-95insTGG
ENST00000696560.1:c.-135-96_-135-95insTGG ENSP00000512718.1:n.-135-96_-135-95insTGG
ENST00000696561.1:c.-135-96_-135-95insTGG ENSP00000512719.1:n.-135-96_-135-95insTGG
ENST00000696562.1:c.-135-96_-135-95insTGG ENSP00000512720.1:n.-135-96_-135-95insTGG
ENST00000603274.1:n.742_743insCCA
XR_926692.1:n.165-96_165-95insTGG