Canonical Allele Identifier: CA449602036
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31357394-G-A
MyVariant Identifiers: chr6:g.31325171G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357394G>A , CM000668.2:g.31357394G>A GRCh38
NC_000006.11:g.31325171G>A , CM000668.1:g.31325171G>A GRCh37
NC_000006.10:g.31433150G>A NCBI36
NG_023187.1:g.4819C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-101C>T
ENST00000481849.6:n.1339-101C>T
ENST00000497377.6:n.1339-101C>T
ENST00000696559.1:c.-135-101C>T ENSP00000512717.1:n.-135-101C>T
ENST00000696560.1:c.-135-101C>T ENSP00000512718.1:n.-135-101C>T
ENST00000696561.1:c.-135-101C>T ENSP00000512719.1:n.-135-101C>T
ENST00000696562.1:c.-135-101C>T ENSP00000512720.1:n.-135-101C>T
ENST00000603274.1:n.748G>A
XR_926692.1:n.165-101C>T