Canonical Allele Identifier: CA2677952643
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31353870-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31353870G>T , CM000668.2:g.31353870G>T GRCh38
NC_000006.11:g.31321647G>T , CM000668.1:g.31321647G>T GRCh37
NC_000006.10:g.31429626G>T NCBI36
NG_023187.1:g.8343C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011514556.1:c.*431C>A XP_011512858.1:n.*431C>A
XM_011514557.1:c.*431C>A XP_011512859.1:n.*431C>A
XR_926175.1:n.1959C>A
NM_005514.7:c.*431C>A NP_005505.2:n.*431C>A
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