Canonical Allele Identifier: CA363311431

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355584-T-A
• MyVariant Identifiers: chr6:g.31323361T>A (hg19) ; chr6:g.31355584T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355584T>A , CM000668.2:g.31355584T>A	GRCh38
NC_000006.11:g.31323361T>A , CM000668.1:g.31323361T>A	GRCh37
NC_000006.10:g.31431340T>A	NCBI36
NG_023187.1:g.6629A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2675A>T
ENST00000481849.6:n.2101A>T
ENST00000497377.6:n.2101A>T
ENST00000640094.2:c.628A>T	ENSP00000491275.2:p.Lys210Ter
ENST00000696558.1:c.697A>T	ENSP00000512716.1:n.697A>T
ENST00000696559.1:c.628A>T	ENSP00000512717.1:p.Lys210Ter
ENST00000696560.1:c.628A>T	ENSP00000512718.1:p.Lys210Ter
ENST00000696561.1:c.628A>T	ENSP00000512719.1:p.Lys210Ter
ENST00000696562.1:c.628A>T	ENSP00000512720.1:p.Lys210Ter
ENST00000412585.7:c.628A>T MANE Select	ENSP00000399168.2:p.Lys210Ter
ENST00000412585.6:c.628A>T	ENSP00000399168.2:p.Lys210Ter
ENST00000434333.1:c.661A>T	ENSP00000405931.1:p.Lys221Ter
ENST00000463574.1:n.219A>T
ENST00000474381.1:n.1077A>T
ENST00000498007.1:n.894A>T
NM_005514.6:c.628A>T	NP_005505.2:p.Lys210Ter
XM_011514556.1:c.661A>T	XP_011512858.1:p.Lys221Ter
XM_011514557.1:c.628A>T	XP_011512859.1:p.Lys210Ter
XR_926175.1:n.1067A>T
NM_005514.7:c.628A>T	NP_005505.2:p.Lys210Ter
NM_005514.8:c.628A>T MANE Select	NP_005505.2:p.Lys210Ter