Canonical Allele Identifier: CA3711202

Gene: HLA-B

Linked Data

• dbSNP Id: rs372726656
• ExAC: 6:31322376 T / C
• gnomAD v2: 6-31322376-T-C
• gnomAD v3: 6-31354599-T-C
• gnomAD v4: 6-31354599-T-C
• MyVariant Identifiers: chr6:g.31322376T>C (hg19) ; chr6:g.31354599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354599T>C , CM000668.2:g.31354599T>C	GRCh38
NC_000006.11:g.31322376T>C , CM000668.1:g.31322376T>C	GRCh37
NC_000006.10:g.31430355T>C	NCBI36
NG_023187.1:g.7614A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3092+34A>G
ENST00000481849.6:n.3052+34A>G
ENST00000497377.6:n.2959+34A>G
ENST00000640094.2:c.928+34A>G	ENSP00000491275.2:n.928+34A>G
ENST00000696558.1:c.1114+34A>G	ENSP00000512716.1:n.1114+34A>G
ENST00000696559.1:c.1045+34A>G	ENSP00000512717.1:n.1045+34A>G
ENST00000696560.1:c.1045+34A>G	ENSP00000512718.1:n.1045+34A>G
ENST00000696561.1:c.1045+34A>G	ENSP00000512719.1:n.1045+34A>G
ENST00000696562.1:c.1045+34A>G	ENSP00000512720.1:n.1045+34A>G
ENST00000412585.7:c.1045+34A>G MANE Select	ENSP00000399168.2:n.1045+34A>G
ENST00000640094.1:c.121+34A>G	ENSP00000491275.1:n.121+34A>G
ENST00000412585.6:c.1045+34A>G	ENSP00000399168.2:n.1045+34A>G
ENST00000481849.5:n.208A>G
ENST00000497377.5:n.444+34A>G
NM_005514.6:c.1045+34A>G	NP_005505.2:n.1045+34A>G
XM_011514556.1:c.1078+34A>G	XP_011512858.1:n.1078+34A>G
XM_011514557.1:c.928+34A>G	XP_011512859.1:n.928+34A>G
XR_926175.1:n.1484+34A>G
NM_005514.7:c.1045+34A>G	NP_005505.2:n.1045+34A>G
NM_005514.8:c.1045+34A>G MANE Select	NP_005505.2:n.1045+34A>G