Canonical Allele Identifier: CA449790997
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs2113754200
gnomAD v4: 6-31357220-C-T
MyVariant Identifiers: chr6:g.31324997C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357220C>T , CM000668.2:g.31357220C>T GRCh38
NC_000006.11:g.31324997C>T , CM000668.1:g.31324997C>T GRCh37
NC_000006.10:g.31432976C>T NCBI36
NG_023187.1:g.4993G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1412G>A
ENST00000481849.6:n.1412G>A
ENST00000497377.6:n.1412G>A
ENST00000696559.1:c.-62G>A ENSP00000512717.1:n.-62G>A
ENST00000696560.1:c.-62G>A ENSP00000512718.1:n.-62G>A
ENST00000696561.1:c.-62G>A ENSP00000512719.1:n.-62G>A
ENST00000696562.1:c.-62G>A ENSP00000512720.1:n.-62G>A
ENST00000603274.1:n.574C>T
NM_005514.7:c.-62G>A NP_005505.2:n.-62G>A
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