Canonical Allele Identifier: CA136832348

Gene: HLA-B

Linked Data

• dbSNP Id: rs41558317
• gnomAD v3: 6-31355073-A-G
• gnomAD v4: 6-31355073-A-G
• MyVariant Identifiers: chr6:g.31322850A>G (hg19) ; chr6:g.31355073A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355073A>G , CM000668.2:g.31355073A>G	GRCh38
NC_000006.11:g.31322850A>G , CM000668.1:g.31322850A>G	GRCh37
NC_000006.10:g.31430829A>G	NCBI36
NG_023187.1:g.7140T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+34T>C
ENST00000481849.6:n.2612T>C
ENST00000497377.6:n.2519T>C
ENST00000640094.2:c.895+244T>C	ENSP00000491275.2:n.895+244T>C
ENST00000696558.1:c.1081+34T>C	ENSP00000512716.1:n.1081+34T>C
ENST00000696559.1:c.1012+34T>C	ENSP00000512717.1:n.1012+34T>C
ENST00000696560.1:c.1012+34T>C	ENSP00000512718.1:n.1012+34T>C
ENST00000696561.1:c.1012+34T>C	ENSP00000512719.1:n.1012+34T>C
ENST00000696562.1:c.1012+34T>C	ENSP00000512720.1:n.1012+34T>C
ENST00000412585.7:c.1012+34T>C MANE Select	ENSP00000399168.2:n.1012+34T>C
ENST00000640094.1:c.88+244T>C	ENSP00000491275.1:n.88+244T>C
ENST00000412585.6:c.1012+34T>C	ENSP00000399168.2:n.1012+34T>C
ENST00000497377.5:n.4T>C
NM_005514.6:c.1012+34T>C	NP_005505.2:n.1012+34T>C
XM_011514556.1:c.1045+34T>C	XP_011512858.1:n.1045+34T>C
XM_011514557.1:c.895+244T>C	XP_011512859.1:n.895+244T>C
XR_926175.1:n.1451+34T>C
NM_005514.7:c.1012+34T>C	NP_005505.2:n.1012+34T>C
NM_005514.8:c.1012+34T>C MANE Select	NP_005505.2:n.1012+34T>C