Canonical Allele Identifier: CA823877582

Gene: HLA-B

Linked Data

• dbSNP Id: rs1335704335
• gnomAD v3: 6-31354546-G-A
• gnomAD v4: 6-31354546-G-A
• MyVariant Identifiers: chr6:g.31322323G>A (hg19) ; chr6:g.31354546G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354546G>A , CM000668.2:g.31354546G>A	GRCh38
NC_000006.11:g.31322323G>A , CM000668.1:g.31322323G>A	GRCh37
NC_000006.10:g.31430302G>A	NCBI36
NG_023187.1:g.7667C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3093-20C>T
ENST00000481849.6:n.3053-20C>T
ENST00000497377.6:n.2960-20C>T
ENST00000640094.2:c.929-20C>T	ENSP00000491275.2:n.929-20C>T
ENST00000696558.1:c.1115-20C>T	ENSP00000512716.1:n.1115-20C>T
ENST00000696559.1:c.1046-20C>T	ENSP00000512717.1:n.1046-20C>T
ENST00000696560.1:c.1046-20C>T	ENSP00000512718.1:n.1046-20C>T
ENST00000696561.1:c.1046-20C>T	ENSP00000512719.1:n.1046-20C>T
ENST00000696562.1:c.1046-20C>T	ENSP00000512720.1:n.1046-20C>T
ENST00000412585.7:c.1046-20C>T MANE Select	ENSP00000399168.2:n.1046-20C>T
ENST00000640094.1:c.122-20C>T	ENSP00000491275.1:n.122-20C>T
ENST00000412585.6:c.1046-20C>T	ENSP00000399168.2:n.1046-20C>T
ENST00000481849.5:n.261C>T
ENST00000497377.5:n.445-20C>T
NM_005514.6:c.1046-20C>T	NP_005505.2:n.1046-20C>T
XM_011514556.1:c.1079-20C>T	XP_011512858.1:n.1079-20C>T
XM_011514557.1:c.929-20C>T	XP_011512859.1:n.929-20C>T
XR_926175.1:n.1485-20C>T
NM_005514.7:c.1046-20C>T	NP_005505.2:n.1046-20C>T
NM_005514.8:c.1046-20C>T MANE Select	NP_005505.2:n.1046-20C>T