Canonical Allele Identifier: CA363309105

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355205-G-T
• gnomAD v4: 6-31355205-G-T
• MyVariant Identifiers: chr6:g.31322982G>T (hg19) ; chr6:g.31355205G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355205G>T , CM000668.2:g.31355205G>T	GRCh38
NC_000006.11:g.31322982G>T , CM000668.1:g.31322982G>T	GRCh37
NC_000006.10:g.31430961G>T	NCBI36
NG_023187.1:g.7008C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2961C>A
ENST00000481849.6:n.2480C>A
ENST00000497377.6:n.2387C>A
ENST00000640094.2:c.895+112C>A	ENSP00000491275.2:n.895+112C>A
ENST00000696558.1:c.983C>A	ENSP00000512716.1:n.983C>A
ENST00000696559.1:c.914C>A	ENSP00000512717.1:p.Thr305Asn
ENST00000696560.1:c.914C>A	ENSP00000512718.1:p.Thr305Asn
ENST00000696561.1:c.914C>A	ENSP00000512719.1:p.Thr305Asn
ENST00000696562.1:c.914C>A	ENSP00000512720.1:p.Thr305Asn
ENST00000412585.7:c.914C>A MANE Select	ENSP00000399168.2:p.Thr305Asn
ENST00000640094.1:c.88+112C>A	ENSP00000491275.1:n.88+112C>A
ENST00000412585.6:c.914C>A	ENSP00000399168.2:p.Thr305Asn
ENST00000463574.1:n.505C>A
NM_005514.6:c.914C>A	NP_005505.2:p.Thr305Asn
XM_011514556.1:c.947C>A	XP_011512858.1:p.Thr316Asn
XM_011514557.1:c.895+112C>A	XP_011512859.1:n.895+112C>A
XR_926175.1:n.1353C>A
NM_005514.7:c.914C>A	NP_005505.2:p.Thr305Asn
NM_005514.8:c.914C>A MANE Select	NP_005505.2:p.Thr305Asn