Canonical Allele Identifier: CA136831094

Gene: HLA-B

Linked Data

• dbSNP Id: rs542419099
• gnomAD v3: 6-31353914-A-G
• gnomAD v4: 6-31353914-A-G
• MyVariant Identifiers: chr6:g.31321691A>G (hg19) ; chr6:g.31353914A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353914A>G , CM000668.2:g.31353914A>G	GRCh38
NC_000006.11:g.31321691A>G , CM000668.1:g.31321691A>G	GRCh37
NC_000006.10:g.31429670A>G	NCBI36
NG_023187.1:g.8299T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3523T>C
ENST00000481849.6:n.3483T>C
ENST00000497377.6:n.3390T>C
ENST00000696558.1:c.1545T>C	ENSP00000512716.1:n.1545T>C
ENST00000696559.1:c.*387T>C	ENSP00000512717.1:n.*387T>C
ENST00000696560.1:c.*387T>C	ENSP00000512718.1:n.*387T>C
ENST00000696561.1:c.*387T>C	ENSP00000512719.1:n.*387T>C
ENST00000696562.1:c.*387T>C	ENSP00000512720.1:n.*387T>C
ENST00000412585.7:c.*387T>C MANE Select	ENSP00000399168.2:n.*387T>C
ENST00000412585.6:c.*387T>C	ENSP00000399168.2:n.*387T>C
ENST00000481849.5:n.711T>C
ENST00000497377.5:n.875T>C
NM_005514.6:c.*387T>C	NP_005505.2:n.*387T>C
XM_011514556.1:c.*387T>C	XP_011512858.1:n.*387T>C
XM_011514557.1:c.*387T>C	XP_011512859.1:n.*387T>C
XR_926175.1:n.1915T>C
NM_005514.7:c.*387T>C	NP_005505.2:n.*387T>C
NM_005514.8:c.*387T>C MANE Select	NP_005505.2:n.*387T>C