Canonical Allele Identifier: CA136831177

Gene: HLA-B

Linked Data

• dbSNP Id: rs951978894
• gnomAD v2: 6-31321809-A-T
• gnomAD v3: 6-31354032-A-T
• gnomAD v4: 6-31354032-A-T
• MyVariant Identifiers: chr6:g.31321809A>T (hg19) ; chr6:g.31354032A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354032A>T , CM000668.2:g.31354032A>T	GRCh38
NC_000006.11:g.31321809A>T , CM000668.1:g.31321809A>T	GRCh37
NC_000006.10:g.31429788A>T	NCBI36
NG_023187.1:g.8181T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3405T>A
ENST00000481849.6:n.3365T>A
ENST00000497377.6:n.3272T>A
ENST00000696558.1:c.1427T>A	ENSP00000512716.1:n.1427T>A
ENST00000696559.1:c.*269T>A	ENSP00000512717.1:n.*269T>A
ENST00000696560.1:c.*269T>A	ENSP00000512718.1:n.*269T>A
ENST00000696561.1:c.*269T>A	ENSP00000512719.1:n.*269T>A
ENST00000696562.1:c.*269T>A	ENSP00000512720.1:n.*269T>A
ENST00000412585.7:c.*269T>A MANE Select	ENSP00000399168.2:n.*269T>A
ENST00000412585.6:c.*269T>A	ENSP00000399168.2:n.*269T>A
ENST00000481849.5:n.593T>A
ENST00000497377.5:n.757T>A
NM_005514.6:c.*269T>A	NP_005505.2:n.*269T>A
XM_011514556.1:c.*269T>A	XP_011512858.1:n.*269T>A
XM_011514557.1:c.*269T>A	XP_011512859.1:n.*269T>A
XR_926175.1:n.1797T>A
NM_005514.7:c.*269T>A	NP_005505.2:n.*269T>A
NM_005514.8:c.*269T>A MANE Select	NP_005505.2:n.*269T>A