Canonical Allele Identifier: CA2677952703

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31353901-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353901T>C , CM000668.2:g.31353901T>C	GRCh38
NC_000006.11:g.31321678T>C , CM000668.1:g.31321678T>C	GRCh37
NC_000006.10:g.31429657T>C	NCBI36
NG_023187.1:g.8312A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3536A>G
ENST00000481849.6:n.3496A>G
ENST00000497377.6:n.3403A>G
ENST00000696558.1:c.1558A>G	ENSP00000512716.1:n.1558A>G
ENST00000696559.1:c.*400A>G	ENSP00000512717.1:n.*400A>G
ENST00000696560.1:c.*400A>G	ENSP00000512718.1:n.*400A>G
ENST00000696561.1:c.*400A>G	ENSP00000512719.1:n.*400A>G
ENST00000696562.1:c.*400A>G	ENSP00000512720.1:n.*400A>G
ENST00000412585.7:c.*400A>G MANE Select	ENSP00000399168.2:n.*400A>G
ENST00000412585.6:c.*400A>G	ENSP00000399168.2:n.*400A>G
ENST00000481849.5:n.724A>G
ENST00000497377.5:n.888A>G
NM_005514.6:c.*400A>G	NP_005505.2:n.*400A>G
XM_011514556.1:c.*400A>G	XP_011512858.1:n.*400A>G
XM_011514557.1:c.*400A>G	XP_011512859.1:n.*400A>G
XR_926175.1:n.1928A>G
NM_005514.7:c.*400A>G	NP_005505.2:n.*400A>G
NM_005514.8:c.*400A>G MANE Select	NP_005505.2:n.*400A>G