Canonical Allele Identifier: CA363315101

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357119-A-T
• MyVariant Identifiers: chr6:g.31324896A>T (hg19) ; chr6:g.31357119A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357119A>T , CM000668.2:g.31357119A>T	GRCh38
NC_000006.11:g.31324896A>T , CM000668.1:g.31324896A>T	GRCh37
NC_000006.10:g.31432875A>T	NCBI36
NG_023187.1:g.5094T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1513T>A
ENST00000481849.6:n.1513T>A
ENST00000497377.6:n.1513T>A
ENST00000640094.2:c.40T>A	ENSP00000491275.2:p.Ser14Thr
ENST00000696558.1:c.40T>A	ENSP00000512716.1:p.Ser14Thr
ENST00000696559.1:c.40T>A	ENSP00000512717.1:p.Ser14Thr
ENST00000696560.1:c.40T>A	ENSP00000512718.1:p.Ser14Thr
ENST00000696561.1:c.40T>A	ENSP00000512719.1:p.Ser14Thr
ENST00000696562.1:c.40T>A	ENSP00000512720.1:p.Ser14Thr
ENST00000412585.7:c.40T>A MANE Select	ENSP00000399168.2:p.Ser14Thr
ENST00000412585.6:c.40T>A	ENSP00000399168.2:p.Ser14Thr
ENST00000434333.1:c.-56T>A	ENSP00000405931.1:n.-56T>A
ENST00000498007.1:n.61T>A
ENST00000603274.1:n.473A>T
NM_005514.6:c.40T>A	NP_005505.2:p.Ser14Thr
XM_011514557.1:c.40T>A	XP_011512859.1:p.Ser14Thr
XR_926175.1:n.50T>A
NM_005514.7:c.40T>A	NP_005505.2:p.Ser14Thr
NM_005514.8:c.40T>A MANE Select	NP_005505.2:p.Ser14Thr