Canonical Allele Identifier: CA363307884

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354497-A-T
• MyVariant Identifiers: chr6:g.31322274A>T (hg19) ; chr6:g.31354497A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354497A>T , CM000668.2:g.31354497A>T	GRCh38
NC_000006.11:g.31322274A>T , CM000668.1:g.31322274A>T	GRCh37
NC_000006.10:g.31430253A>T	NCBI36
NG_023187.1:g.7716T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3122T>A
ENST00000481849.6:n.3082T>A
ENST00000497377.6:n.2989T>A
ENST00000640094.2:c.958T>A	ENSP00000491275.2:p.Ser320Thr
ENST00000696558.1:c.1144T>A	ENSP00000512716.1:n.1144T>A
ENST00000696559.1:c.1075T>A	ENSP00000512717.1:p.Ser359Thr
ENST00000696560.1:c.1075T>A	ENSP00000512718.1:p.Ser359Thr
ENST00000696561.1:c.1075T>A	ENSP00000512719.1:p.Ser359Thr
ENST00000696562.1:c.1075T>A	ENSP00000512720.1:p.Ser359Thr
ENST00000412585.7:c.1075T>A MANE Select	ENSP00000399168.2:p.Ser359Thr
ENST00000412585.6:c.1075T>A	ENSP00000399168.2:p.Ser359Thr
ENST00000481849.5:n.310T>A
ENST00000497377.5:n.474T>A
NM_005514.6:c.1075T>A	NP_005505.2:p.Ser359Thr
XM_011514556.1:c.1108T>A	XP_011512858.1:p.Ser370Thr
XM_011514557.1:c.958T>A	XP_011512859.1:p.Ser320Thr
XR_926175.1:n.1514T>A
NM_005514.7:c.1075T>A	NP_005505.2:p.Ser359Thr
NM_005514.8:c.1075T>A MANE Select	NP_005505.2:p.Ser359Thr