Canonical Allele Identifier: CA1087466097

Gene: HLA-B

Linked Data

• dbSNP Id: rs41555513
• gnomAD v3: 6-31355703-G-C
• gnomAD v4: 6-31355703-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355703G>C , CM000668.2:g.31355703G>C	GRCh38
NC_000006.11:g.31323480G>C , CM000668.1:g.31323480G>C	GRCh37
NC_000006.10:g.31431459G>C	NCBI36
NG_023187.1:g.6510C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2556C>G
ENST00000481849.6:n.2093-111C>G
ENST00000497377.6:n.2093-111C>G
ENST00000640094.2:c.620-111C>G	ENSP00000491275.2:n.620-111C>G
ENST00000696558.1:c.688+35C>G	ENSP00000512716.1:n.688+35C>G
ENST00000696559.1:c.620-111C>G	ENSP00000512717.1:n.620-111C>G
ENST00000696560.1:c.620-111C>G	ENSP00000512718.1:n.620-111C>G
ENST00000696561.1:c.620-111C>G	ENSP00000512719.1:n.620-111C>G
ENST00000696562.1:c.620-111C>G	ENSP00000512720.1:n.620-111C>G
ENST00000412585.7:c.620-111C>G MANE Select	ENSP00000399168.2:n.620-111C>G
ENST00000412585.6:c.620-111C>G	ENSP00000399168.2:n.620-111C>G
ENST00000434333.1:c.653-111C>G	ENSP00000405931.1:n.653-111C>G
ENST00000463574.1:n.100C>G
ENST00000474381.1:n.958C>G
ENST00000498007.1:n.886-111C>G
NM_005514.6:c.620-111C>G	NP_005505.2:n.620-111C>G
XM_011514556.1:c.653-111C>G	XP_011512858.1:n.653-111C>G
XM_011514557.1:c.620-111C>G	XP_011512859.1:n.620-111C>G
XR_926175.1:n.1058+35C>G
NM_005514.7:c.620-111C>G	NP_005505.2:n.620-111C>G
NM_005514.8:c.620-111C>G MANE Select	NP_005505.2:n.620-111C>G