Canonical Allele Identifier: CA566340313
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1446863353
gnomAD v2: 6-31327086-C-T
gnomAD v3: 6-31359309-C-T
gnomAD v4: 6-31359309-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359309C>T , CM000668.2:g.31359309C>T GRCh38
NC_000006.11:g.31327086C>T , CM000668.1:g.31327086C>T GRCh37
NC_000006.10:g.31435065C>T NCBI36
NG_023187.1:g.2904G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1271-1628G>A
ENST00000481849.6:n.1271-1628G>A
ENST00000497377.6:n.1271-1628G>A
ENST00000696559.1:c.-203-1628G>A ENSP00000512717.1:n.-203-1628G>A
ENST00000696560.1:c.-203-1628G>A ENSP00000512718.1:n.-203-1628G>A
ENST00000696561.1:c.-203-1628G>A ENSP00000512719.1:n.-203-1628G>A
ENST00000696562.1:c.-135-2016G>A ENSP00000512720.1:n.-135-2016G>A