Canonical Allele Identifier: CA1087463581

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766778872
• gnomAD v3: 6-31354975-A-G
• gnomAD v4: 6-31354975-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354975A>G , CM000668.2:g.31354975A>G	GRCh38
NC_000006.11:g.31322752A>G , CM000668.1:g.31322752A>G	GRCh37
NC_000006.10:g.31430731A>G	NCBI36
NG_023187.1:g.7238T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+132T>C
ENST00000481849.6:n.2710T>C
ENST00000497377.6:n.2617T>C
ENST00000640094.2:c.896-310T>C	ENSP00000491275.2:n.896-310T>C
ENST00000696558.1:c.1081+132T>C	ENSP00000512716.1:n.1081+132T>C
ENST00000696559.1:c.1012+132T>C	ENSP00000512717.1:n.1012+132T>C
ENST00000696560.1:c.1012+132T>C	ENSP00000512718.1:n.1012+132T>C
ENST00000696561.1:c.1012+132T>C	ENSP00000512719.1:n.1012+132T>C
ENST00000696562.1:c.1012+132T>C	ENSP00000512720.1:n.1012+132T>C
ENST00000412585.7:c.1012+132T>C MANE Select	ENSP00000399168.2:n.1012+132T>C
ENST00000640094.1:c.89-310T>C	ENSP00000491275.1:n.89-310T>C
ENST00000412585.6:c.1012+132T>C	ENSP00000399168.2:n.1012+132T>C
ENST00000497377.5:n.102T>C
NM_005514.6:c.1012+132T>C	NP_005505.2:n.1012+132T>C
XM_011514556.1:c.1045+132T>C	XP_011512858.1:n.1045+132T>C
XM_011514557.1:c.896-310T>C	XP_011512859.1:n.896-310T>C
XR_926175.1:n.1451+132T>C
NM_005514.7:c.1012+132T>C	NP_005505.2:n.1012+132T>C
NM_005514.8:c.1012+132T>C MANE Select	NP_005505.2:n.1012+132T>C