Canonical Allele Identifier: CA2677958242
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31357441-TCCCTCTTCTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357443_31357452del , CM000668.2:g.31357443_31357452del GRCh38
NC_000006.11:g.31325220_31325229del , CM000668.1:g.31325220_31325229del GRCh37
NC_000006.10:g.31433199_31433208del NCBI36
NG_023187.1:g.4762_4771del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-158_1339-149del
ENST00000481849.6:n.1339-158_1339-149del
ENST00000497377.6:n.1339-158_1339-149del
ENST00000696559.1:c.-135-158_-135-149del ENSP00000512717.1:n.-135-158_-135-149del
ENST00000696560.1:c.-135-158_-135-149del ENSP00000512718.1:n.-135-158_-135-149del
ENST00000696561.1:c.-135-158_-135-149del ENSP00000512719.1:n.-135-158_-135-149del
ENST00000696562.1:c.-135-158_-135-149del ENSP00000512720.1:n.-135-158_-135-149del
ENST00000603274.1:n.797_806del
XR_926692.1:n.165-158_165-149del
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