Canonical Allele Identifier: CA449790715

Gene: HLA-B

Linked Data

• dbSNP Id: rs78135486
• gnomAD v2: 6-31323329-G-A
• gnomAD v4: 6-31355552-G-A
• MyVariant Identifiers: chr6:g.31323329G>A (hg19) ; chr6:g.31355552G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355552G>A , CM000668.2:g.31355552G>A	GRCh38
NC_000006.11:g.31323329G>A , CM000668.1:g.31323329G>A	GRCh37
NC_000006.10:g.31431308G>A	NCBI36
NG_023187.1:g.6661C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2707C>T
ENST00000481849.6:n.2133C>T
ENST00000497377.6:n.2133C>T
ENST00000640094.2:c.660C>T	ENSP00000491275.2:p.Asp220=
ENST00000696558.1:c.729C>T	ENSP00000512716.1:n.729C>T
ENST00000696559.1:c.660C>T	ENSP00000512717.1:p.Asp220=
ENST00000696560.1:c.660C>T	ENSP00000512718.1:p.Asp220=
ENST00000696561.1:c.660C>T	ENSP00000512719.1:p.Asp220=
ENST00000696562.1:c.660C>T	ENSP00000512720.1:p.Asp220=
ENST00000412585.7:c.660C>T MANE Select	ENSP00000399168.2:p.Asp220=
ENST00000412585.6:c.660C>T	ENSP00000399168.2:p.Asp220=
ENST00000434333.1:c.693C>T	ENSP00000405931.1:p.Asp231=
ENST00000463574.1:n.251C>T
ENST00000474381.1:n.1109C>T
ENST00000498007.1:n.926C>T
NM_005514.6:c.660C>T	NP_005505.2:p.Asp220=
XM_011514556.1:c.693C>T	XP_011512858.1:p.Asp231=
XM_011514557.1:c.660C>T	XP_011512859.1:p.Asp220=
XR_926175.1:n.1099C>T
NM_005514.7:c.660C>T	NP_005505.2:p.Asp220=
NM_005514.8:c.660C>T MANE Select	NP_005505.2:p.Asp220=