Canonical Allele Identifier: CA449790896
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs949147688
gnomAD v2: 6-31324963-G-T
gnomAD v3: 6-31357186-G-T
gnomAD v4: 6-31357186-G-T
MyVariant Identifiers: chr6:g.31324963G>T (hg19) chr6:g.31357186G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357186G>T , CM000668.2:g.31357186G>T GRCh38
NC_000006.11:g.31324963G>T , CM000668.1:g.31324963G>T GRCh37
NC_000006.10:g.31432942G>T NCBI36
NG_023187.1:g.5027C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1446C>A
ENST00000481849.6:n.1446C>A
ENST00000497377.6:n.1446C>A
ENST00000696559.1:c.-28C>A ENSP00000512717.1:n.-28C>A
ENST00000696560.1:c.-28C>A ENSP00000512718.1:n.-28C>A
ENST00000696561.1:c.-28C>A ENSP00000512719.1:n.-28C>A
ENST00000696562.1:c.-28C>A ENSP00000512720.1:n.-28C>A
ENST00000412585.6:c.-28C>A ENSP00000399168.2:n.-28C>A
ENST00000434333.1:c.-123C>A ENSP00000405931.1:n.-123C>A
ENST00000603274.1:n.540G>T
NM_005514.6:c.-28C>A NP_005505.2:n.-28C>A
NM_005514.7:c.-28C>A NP_005505.2:n.-28C>A
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