Canonical Allele Identifier: CA3711083

Gene: HLA-B

Linked Data

• dbSNP Id: rs151341415
• ExAC: 6:31322210 C / G
• gnomAD v2: 6-31322210-C-G
• gnomAD v3: 6-31354433-C-G
• gnomAD v4: 6-31354433-C-G
• MyVariant Identifiers: chr6:g.31322210C>G (hg19) ; chr6:g.31322210_31322217delinsGCCCCAGA (hg19) ; chr6:g.31354433C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354433C>G , CM000668.2:g.31354433C>G	GRCh38
NC_000006.11:g.31322210C>G , CM000668.1:g.31322210C>G	GRCh37
NC_000006.10:g.31430189C>G	NCBI36
NG_023187.1:g.7780G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3140+46G>C
ENST00000481849.6:n.3100+46G>C
ENST00000497377.6:n.3007+46G>C
ENST00000696558.1:c.1162+46G>C	ENSP00000512716.1:n.1162+46G>C
ENST00000696559.1:c.*4+46G>C	ENSP00000512717.1:n.*4+46G>C
ENST00000696560.1:c.*4+46G>C	ENSP00000512718.1:n.*4+46G>C
ENST00000696561.1:c.*4+46G>C	ENSP00000512719.1:n.*4+46G>C
ENST00000696562.1:c.*4+46G>C	ENSP00000512720.1:n.*4+46G>C
ENST00000412585.7:c.*4+46G>C MANE Select	ENSP00000399168.2:n.*4+46G>C
ENST00000412585.6:c.*4+46G>C	ENSP00000399168.2:n.*4+46G>C
ENST00000481849.5:n.328+46G>C
ENST00000497377.5:n.492+46G>C
NM_005514.6:c.*4+46G>C	NP_005505.2:n.*4+46G>C
XM_011514556.1:c.*4+46G>C	XP_011512858.1:n.*4+46G>C
XM_011514557.1:c.*4+46G>C	XP_011512859.1:n.*4+46G>C
XR_926175.1:n.1532+46G>C
NM_005514.7:c.*4+46G>C	NP_005505.2:n.*4+46G>C
NM_005514.8:c.*4+46G>C MANE Select	NP_005505.2:n.*4+46G>C