Canonical Allele Identifier: CA2580592235

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353908A>T , CM000668.2:g.31353908A>T	GRCh38
NC_000006.11:g.31321685A>T , CM000668.1:g.31321685A>T	GRCh37
NC_000006.10:g.31429664A>T	NCBI36
NG_023187.1:g.8305T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3529T>A
ENST00000481849.6:n.3489T>A
ENST00000497377.6:n.3396T>A
ENST00000696558.1:c.1551T>A	ENSP00000512716.1:n.1551T>A
ENST00000696559.1:c.*393T>A	ENSP00000512717.1:n.*393T>A
ENST00000696560.1:c.*393T>A	ENSP00000512718.1:n.*393T>A
ENST00000696561.1:c.*393T>A	ENSP00000512719.1:n.*393T>A
ENST00000696562.1:c.*393T>A	ENSP00000512720.1:n.*393T>A
ENST00000412585.7:c.*393T>A MANE Select	ENSP00000399168.2:n.*393T>A
ENST00000412585.6:c.*393T>A	ENSP00000399168.2:n.*393T>A
ENST00000481849.5:n.717T>A
ENST00000497377.5:n.881T>A
NM_005514.6:c.*393T>A	NP_005505.2:n.*393T>A
XM_011514556.1:c.*393T>A	XP_011512858.1:n.*393T>A
XM_011514557.1:c.*393T>A	XP_011512859.1:n.*393T>A
XR_926175.1:n.1921T>A
NM_005514.7:c.*393T>A	NP_005505.2:n.*393T>A
NM_005514.8:c.*393T>A MANE Select	NP_005505.2:n.*393T>A