Canonical Allele Identifier: CA3711210

Gene: HLA-B

Linked Data

• dbSNP Id: rs763742111
• ExAC: 6:31322398 C / G
• gnomAD v2: 6-31322398-C-G
• gnomAD v3: 6-31354621-C-G
• gnomAD v4: 6-31354621-C-G
• MyVariant Identifiers: chr6:g.31322398C>G (hg19) ; chr6:g.31354621C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354621C>G , CM000668.2:g.31354621C>G	GRCh38
NC_000006.11:g.31322398C>G , CM000668.1:g.31322398C>G	GRCh37
NC_000006.10:g.31430377C>G	NCBI36
NG_023187.1:g.7592G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3092+12G>C
ENST00000481849.6:n.3052+12G>C
ENST00000497377.6:n.2959+12G>C
ENST00000640094.2:c.928+12G>C	ENSP00000491275.2:n.928+12G>C
ENST00000696558.1:c.1114+12G>C	ENSP00000512716.1:n.1114+12G>C
ENST00000696559.1:c.1045+12G>C	ENSP00000512717.1:n.1045+12G>C
ENST00000696560.1:c.1045+12G>C	ENSP00000512718.1:n.1045+12G>C
ENST00000696561.1:c.1045+12G>C	ENSP00000512719.1:n.1045+12G>C
ENST00000696562.1:c.1045+12G>C	ENSP00000512720.1:n.1045+12G>C
ENST00000412585.7:c.1045+12G>C MANE Select	ENSP00000399168.2:n.1045+12G>C
ENST00000640094.1:c.121+12G>C	ENSP00000491275.1:n.121+12G>C
ENST00000412585.6:c.1045+12G>C	ENSP00000399168.2:n.1045+12G>C
ENST00000481849.5:n.186G>C
ENST00000497377.5:n.444+12G>C
NM_005514.6:c.1045+12G>C	NP_005505.2:n.1045+12G>C
XM_011514556.1:c.1078+12G>C	XP_011512858.1:n.1078+12G>C
XM_011514557.1:c.928+12G>C	XP_011512859.1:n.928+12G>C
XR_926175.1:n.1484+12G>C
NM_005514.7:c.1045+12G>C	NP_005505.2:n.1045+12G>C
NM_005514.8:c.1045+12G>C MANE Select	NP_005505.2:n.1045+12G>C