Canonical Allele Identifier: CA363308197

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354645-A-T
• MyVariant Identifiers: chr6:g.31322422A>T (hg19) ; chr6:g.31354645A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354645A>T , CM000668.2:g.31354645A>T	GRCh38
NC_000006.11:g.31322422A>T , CM000668.1:g.31322422A>T	GRCh37
NC_000006.10:g.31430401A>T	NCBI36
NG_023187.1:g.7568T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3080T>A
ENST00000481849.6:n.3040T>A
ENST00000497377.6:n.2947T>A
ENST00000640094.2:c.916T>A	ENSP00000491275.2:p.Ser306Thr
ENST00000696558.1:c.1102T>A	ENSP00000512716.1:n.1102T>A
ENST00000696559.1:c.1033T>A	ENSP00000512717.1:p.Ser345Thr
ENST00000696560.1:c.1033T>A	ENSP00000512718.1:p.Ser345Thr
ENST00000696561.1:c.1033T>A	ENSP00000512719.1:p.Ser345Thr
ENST00000696562.1:c.1033T>A	ENSP00000512720.1:p.Ser345Thr
ENST00000412585.7:c.1033T>A MANE Select	ENSP00000399168.2:p.Ser345Thr
ENST00000640094.1:c.109T>A	ENSP00000491275.1:p.Ser37Thr
ENST00000412585.6:c.1033T>A	ENSP00000399168.2:p.Ser345Thr
ENST00000481849.5:n.162T>A
ENST00000497377.5:n.432T>A
NM_005514.6:c.1033T>A	NP_005505.2:p.Ser345Thr
XM_011514556.1:c.1066T>A	XP_011512858.1:p.Ser356Thr
XM_011514557.1:c.916T>A	XP_011512859.1:p.Ser306Thr
XR_926175.1:n.1472T>A
NM_005514.7:c.1033T>A	NP_005505.2:p.Ser345Thr
NM_005514.8:c.1033T>A MANE Select	NP_005505.2:p.Ser345Thr