Canonical Allele Identifier: CA3711110

Gene: HLA-B

Linked Data

• dbSNP Id: rs151341413
• ExAC: 6:31322215 A / C
• gnomAD v2: 6-31322215-A-C
• gnomAD v3: 6-31354438-A-C
• gnomAD v4: 6-31354438-A-C
• MyVariant Identifiers: chr6:g.31322215A>C (hg19) ; chr6:g.31322215_31322216delinsCG (hg19) ; chr6:g.31322215_31322219delinsCGACC (hg19) ; chr6:g.31354438A>C (hg38) ; chr6:g.31354438_31354439delinsCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354438A>C , CM000668.2:g.31354438A>C	GRCh38
NC_000006.11:g.31322215A>C , CM000668.1:g.31322215A>C	GRCh37
NC_000006.10:g.31430194A>C	NCBI36
NG_023187.1:g.7775T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3140+41T>G
ENST00000481849.6:n.3100+41T>G
ENST00000497377.6:n.3007+41T>G
ENST00000696558.1:c.1162+41T>G	ENSP00000512716.1:n.1162+41T>G
ENST00000696559.1:c.*4+41T>G	ENSP00000512717.1:n.*4+41T>G
ENST00000696560.1:c.*4+41T>G	ENSP00000512718.1:n.*4+41T>G
ENST00000696561.1:c.*4+41T>G	ENSP00000512719.1:n.*4+41T>G
ENST00000696562.1:c.*4+41T>G	ENSP00000512720.1:n.*4+41T>G
ENST00000412585.7:c.*4+41T>G MANE Select	ENSP00000399168.2:n.*4+41T>G
ENST00000412585.6:c.*4+41T>G	ENSP00000399168.2:n.*4+41T>G
ENST00000481849.5:n.328+41T>G
ENST00000497377.5:n.492+41T>G
NM_005514.6:c.*4+41T>G	NP_005505.2:n.*4+41T>G
XM_011514556.1:c.*4+41T>G	XP_011512858.1:n.*4+41T>G
XM_011514557.1:c.*4+41T>G	XP_011512859.1:n.*4+41T>G
XR_926175.1:n.1532+41T>G
NM_005514.7:c.*4+41T>G	NP_005505.2:n.*4+41T>G
NM_005514.8:c.*4+41T>G MANE Select	NP_005505.2:n.*4+41T>G