Canonical Allele Identifier: CA449603840
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1241026023
gnomAD v3: 6-31357599-C-T
gnomAD v4: 6-31357599-C-T
MyVariant Identifiers: chr6:g.31325376C>T (hg19) chr6:g.31357599C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357599C>T , CM000668.2:g.31357599C>T GRCh38
NC_000006.11:g.31325376C>T , CM000668.1:g.31325376C>T GRCh37
NC_000006.10:g.31433355C>T NCBI36
NG_023187.1:g.4614G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+15G>A
ENST00000481849.6:n.1338+15G>A
ENST00000497377.6:n.1338+15G>A
ENST00000696559.1:c.-136+15G>A ENSP00000512717.1:n.-136+15G>A
ENST00000696560.1:c.-136+15G>A ENSP00000512718.1:n.-136+15G>A
ENST00000696561.1:c.-136+15G>A ENSP00000512719.1:n.-136+15G>A
ENST00000696562.1:c.-135-306G>A ENSP00000512720.1:n.-135-306G>A
ENST00000603274.1:n.953C>T
XR_926692.1:n.164+15G>A
Search 100 bp 5'
Search 100 bp 3'