Canonical Allele Identifier: CA3711473

Gene: HLA-B

Linked Data

• dbSNP Id: rs201073969
• ExAC: 6:31323908 T / C
• gnomAD v2: 6-31323908-T-C
• gnomAD v3: 6-31356131-T-C
• gnomAD v4: 6-31356131-T-C
• MyVariant Identifiers: chr6:g.31323908T>C (hg19) ; chr6:g.31356131T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356131T>C , CM000668.2:g.31356131T>C	GRCh38
NC_000006.11:g.31323908T>C , CM000668.1:g.31323908T>C	GRCh37
NC_000006.10:g.31431887T>C	NCBI36
NG_023187.1:g.6082A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2128A>G
ENST00000481849.6:n.2092+36A>G
ENST00000497377.6:n.2092+36A>G
ENST00000640094.2:c.619+36A>G	ENSP00000491275.2:n.619+36A>G
ENST00000696558.1:c.619+36A>G	ENSP00000512716.1:n.619+36A>G
ENST00000696559.1:c.619+36A>G	ENSP00000512717.1:n.619+36A>G
ENST00000696560.1:c.619+36A>G	ENSP00000512718.1:n.619+36A>G
ENST00000696561.1:c.619+36A>G	ENSP00000512719.1:n.619+36A>G
ENST00000696562.1:c.619+36A>G	ENSP00000512720.1:n.619+36A>G
ENST00000412585.7:c.619+36A>G MANE Select	ENSP00000399168.2:n.619+36A>G
ENST00000412585.6:c.619+36A>G	ENSP00000399168.2:n.619+36A>G
ENST00000434333.1:c.652+36A>G	ENSP00000405931.1:n.652+36A>G
ENST00000474381.1:n.530A>G
ENST00000498007.1:n.885+36A>G
NM_005514.6:c.619+36A>G	NP_005505.2:n.619+36A>G
XM_011514556.1:c.652+36A>G	XP_011512858.1:n.652+36A>G
XM_011514557.1:c.619+36A>G	XP_011512859.1:n.619+36A>G
XR_926175.1:n.665A>G
NM_005514.7:c.619+36A>G	NP_005505.2:n.619+36A>G
NM_005514.8:c.619+36A>G MANE Select	NP_005505.2:n.619+36A>G