Canonical Allele Identifier: CA2770505937

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353903T>A , CM000668.2:g.31353903T>A	GRCh38
NC_000006.11:g.31321680T>A , CM000668.1:g.31321680T>A	GRCh37
NC_000006.10:g.31429659T>A	NCBI36
NG_023187.1:g.8310A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3534A>T
ENST00000481849.6:n.3494A>T
ENST00000497377.6:n.3401A>T
ENST00000696558.1:c.1556A>T	ENSP00000512716.1:n.1556A>T
ENST00000696559.1:c.*398A>T	ENSP00000512717.1:n.*398A>T
ENST00000696560.1:c.*398A>T	ENSP00000512718.1:n.*398A>T
ENST00000696561.1:c.*398A>T	ENSP00000512719.1:n.*398A>T
ENST00000696562.1:c.*398A>T	ENSP00000512720.1:n.*398A>T
ENST00000412585.7:c.*398A>T MANE Select	ENSP00000399168.2:n.*398A>T
ENST00000412585.6:c.*398A>T	ENSP00000399168.2:n.*398A>T
ENST00000481849.5:n.722A>T
ENST00000497377.5:n.886A>T
NM_005514.6:c.*398A>T	NP_005505.2:n.*398A>T
XM_011514556.1:c.*398A>T	XP_011512858.1:n.*398A>T
XM_011514557.1:c.*398A>T	XP_011512859.1:n.*398A>T
XR_926175.1:n.1926A>T
NM_005514.7:c.*398A>T	NP_005505.2:n.*398A>T
NM_005514.8:c.*398A>T MANE Select	NP_005505.2:n.*398A>T