Canonical Allele Identifier: CA3711183

Gene: HLA-B

Linked Data

• dbSNP Id: rs371899158
• ExAC: 6:31322315 C / T
• gnomAD v2: 6-31322315-C-T
• gnomAD v3: 6-31354538-C-T
• gnomAD v4: 6-31354538-C-T
• MyVariant Identifiers: chr6:g.31322315C>T (hg19) ; chr6:g.31354538C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354538C>T , CM000668.2:g.31354538C>T	GRCh38
NC_000006.11:g.31322315C>T , CM000668.1:g.31322315C>T	GRCh37
NC_000006.10:g.31430294C>T	NCBI36
NG_023187.1:g.7675G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3093-12G>A
ENST00000481849.6:n.3053-12G>A
ENST00000497377.6:n.2960-12G>A
ENST00000640094.2:c.929-12G>A	ENSP00000491275.2:n.929-12G>A
ENST00000696558.1:c.1115-12G>A	ENSP00000512716.1:n.1115-12G>A
ENST00000696559.1:c.1046-12G>A	ENSP00000512717.1:n.1046-12G>A
ENST00000696560.1:c.1046-12G>A	ENSP00000512718.1:n.1046-12G>A
ENST00000696561.1:c.1046-12G>A	ENSP00000512719.1:n.1046-12G>A
ENST00000696562.1:c.1046-12G>A	ENSP00000512720.1:n.1046-12G>A
ENST00000412585.7:c.1046-12G>A MANE Select	ENSP00000399168.2:n.1046-12G>A
ENST00000640094.1:c.122-12G>A	ENSP00000491275.1:n.122-12G>A
ENST00000412585.6:c.1046-12G>A	ENSP00000399168.2:n.1046-12G>A
ENST00000481849.5:n.269G>A
ENST00000497377.5:n.445-12G>A
NM_005514.6:c.1046-12G>A	NP_005505.2:n.1046-12G>A
XM_011514556.1:c.1079-12G>A	XP_011512858.1:n.1079-12G>A
XM_011514557.1:c.929-12G>A	XP_011512859.1:n.929-12G>A
XR_926175.1:n.1485-12G>A
NM_005514.7:c.1046-12G>A	NP_005505.2:n.1046-12G>A
NM_005514.8:c.1046-12G>A MANE Select	NP_005505.2:n.1046-12G>A