Canonical Allele Identifier: CA363314981

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357090-C-T
• MyVariant Identifiers: chr6:g.31324867C>T (hg19) ; chr6:g.31357090C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357090C>T , CM000668.2:g.31357090C>T	GRCh38
NC_000006.11:g.31324867C>T , CM000668.1:g.31324867C>T	GRCh37
NC_000006.10:g.31432846C>T	NCBI36
NG_023187.1:g.5123G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1542G>A
ENST00000481849.6:n.1542G>A
ENST00000497377.6:n.1542G>A
ENST00000640094.2:c.69G>A	ENSP00000491275.2:p.Trp23Ter
ENST00000696558.1:c.69G>A	ENSP00000512716.1:p.Trp23Ter
ENST00000696559.1:c.69G>A	ENSP00000512717.1:p.Trp23Ter
ENST00000696560.1:c.69G>A	ENSP00000512718.1:p.Trp23Ter
ENST00000696561.1:c.69G>A	ENSP00000512719.1:p.Trp23Ter
ENST00000696562.1:c.69G>A	ENSP00000512720.1:p.Trp23Ter
ENST00000412585.7:c.69G>A MANE Select	ENSP00000399168.2:p.Trp23Ter
ENST00000412585.6:c.69G>A	ENSP00000399168.2:p.Trp23Ter
ENST00000434333.1:c.-27G>A	ENSP00000405931.1:n.-27G>A
ENST00000498007.1:n.90G>A
ENST00000603274.1:n.444C>T
NM_005514.6:c.69G>A	NP_005505.2:p.Trp23Ter
XM_011514557.1:c.69G>A	XP_011512859.1:p.Trp23Ter
XR_926175.1:n.79G>A
NM_005514.7:c.69G>A	NP_005505.2:p.Trp23Ter
NM_005514.8:c.69G>A MANE Select	NP_005505.2:p.Trp23Ter