Canonical Allele Identifier: CA15467004

Gene: HLA-B

Linked Data

• dbSNP Id: rs878941341
• gnomAD v2: 6-31321694-A-G
• gnomAD v3: 6-31353917-A-G
• gnomAD v4: 6-31353917-A-G
• MyVariant Identifiers: chr6:g.31321694A>G (hg19) ; chr6:g.31353917A>G (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353917A>G , CM000668.2:g.31353917A>G	GRCh38
NC_000006.11:g.31321694A>G , CM000668.1:g.31321694A>G	GRCh37
NC_000006.10:g.31429673A>G	NCBI36
NG_023187.1:g.8296T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3520T>C
ENST00000481849.6:n.3480T>C
ENST00000497377.6:n.3387T>C
ENST00000696558.1:c.1542T>C	ENSP00000512716.1:n.1542T>C
ENST00000696559.1:c.*384T>C	ENSP00000512717.1:n.*384T>C
ENST00000696560.1:c.*384T>C	ENSP00000512718.1:n.*384T>C
ENST00000696561.1:c.*384T>C	ENSP00000512719.1:n.*384T>C
ENST00000696562.1:c.*384T>C	ENSP00000512720.1:n.*384T>C
ENST00000412585.7:c.*384T>C MANE Select	ENSP00000399168.2:n.*384T>C
ENST00000412585.6:c.*384T>C	ENSP00000399168.2:n.*384T>C
ENST00000481849.5:n.708T>C
ENST00000497377.5:n.872T>C
NM_005514.6:c.*384T>C	NP_005505.2:n.*384T>C
XM_011514556.1:c.*384T>C	XP_011512858.1:n.*384T>C
XM_011514557.1:c.*384T>C	XP_011512859.1:n.*384T>C
XR_926175.1:n.1912T>C
NM_005514.7:c.*384T>C	NP_005505.2:n.*384T>C
NM_005514.8:c.*384T>C MANE Select	NP_005505.2:n.*384T>C