Canonical Allele Identifier: CA12320880
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs2596490
gnomAD v2: 6-31324996-G-C
gnomAD v3: 6-31357219-G-C
gnomAD v4: 6-31357219-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357219G>C , CM000668.2:g.31357219G>C GRCh38
NC_000006.11:g.31324996G>C , CM000668.1:g.31324996G>C GRCh37
NC_000006.10:g.31432975G>C NCBI36
NG_023187.1:g.4994C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1413C>G
ENST00000481849.6:n.1413C>G
ENST00000497377.6:n.1413C>G
ENST00000696559.1:c.-61C>G ENSP00000512717.1:n.-61C>G
ENST00000696560.1:c.-61C>G ENSP00000512718.1:n.-61C>G
ENST00000696561.1:c.-61C>G ENSP00000512719.1:n.-61C>G
ENST00000696562.1:c.-61C>G ENSP00000512720.1:n.-61C>G
ENST00000603274.1:n.573G>C
NM_005514.7:c.-61C>G NP_005505.2:n.-61C>G