Canonical Allele Identifier: CA449790947
Gene: HLA-B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31324980C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357203C>G , CM000668.2:g.31357203C>G GRCh38
NC_000006.11:g.31324980C>G , CM000668.1:g.31324980C>G GRCh37
NC_000006.10:g.31432959C>G NCBI36
NG_023187.1:g.5010G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1429G>C
ENST00000481849.6:n.1429G>C
ENST00000497377.6:n.1429G>C
ENST00000696559.1:c.-45G>C ENSP00000512717.1:n.-45G>C
ENST00000696560.1:c.-45G>C ENSP00000512718.1:n.-45G>C
ENST00000696561.1:c.-45G>C ENSP00000512719.1:n.-45G>C
ENST00000696562.1:c.-45G>C ENSP00000512720.1:n.-45G>C
ENST00000603274.1:n.557C>G
NM_005514.6:c.-45G>C NP_005505.2:n.-45G>C
NM_005514.7:c.-45G>C NP_005505.2:n.-45G>C
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