Canonical Allele Identifier: CA136833265

Gene: HLA-B

Linked Data

• dbSNP Id: rs41552112
• gnomAD v2: 6-31323736-T-A
• gnomAD v3: 6-31355959-T-A
• gnomAD v4: 6-31355959-T-A
• MyVariant Identifiers: chr6:g.31323736T>A (hg19) ; chr6:g.31355959T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355959T>A , CM000668.2:g.31355959T>A	GRCh38
NC_000006.11:g.31323736T>A , CM000668.1:g.31323736T>A	GRCh37
NC_000006.10:g.31431715T>A	NCBI36
NG_023187.1:g.6254A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2300A>T
ENST00000481849.6:n.2092+208A>T
ENST00000497377.6:n.2092+208A>T
ENST00000640094.2:c.619+208A>T	ENSP00000491275.2:n.619+208A>T
ENST00000696558.1:c.620-153A>T	ENSP00000512716.1:n.620-153A>T
ENST00000696559.1:c.619+208A>T	ENSP00000512717.1:n.619+208A>T
ENST00000696560.1:c.619+208A>T	ENSP00000512718.1:n.619+208A>T
ENST00000696561.1:c.619+208A>T	ENSP00000512719.1:n.619+208A>T
ENST00000696562.1:c.619+208A>T	ENSP00000512720.1:n.619+208A>T
ENST00000412585.7:c.619+208A>T MANE Select	ENSP00000399168.2:n.619+208A>T
ENST00000412585.6:c.619+208A>T	ENSP00000399168.2:n.619+208A>T
ENST00000434333.1:c.652+208A>T	ENSP00000405931.1:n.652+208A>T
ENST00000474381.1:n.702A>T
ENST00000498007.1:n.885+208A>T
NM_005514.6:c.619+208A>T	NP_005505.2:n.619+208A>T
XM_011514556.1:c.652+208A>T	XP_011512858.1:n.652+208A>T
XM_011514557.1:c.619+208A>T	XP_011512859.1:n.619+208A>T
XR_926175.1:n.837A>T
NM_005514.7:c.619+208A>T	NP_005505.2:n.619+208A>T
NM_005514.8:c.619+208A>T MANE Select	NP_005505.2:n.619+208A>T