Canonical Allele Identifier: CA3711237

Gene: HLA-B

Linked Data

• dbSNP Id: rs754453115
• ExAC: 6:31322843 G / T
• gnomAD v2: 6-31322843-G-T
• gnomAD v3: 6-31355066-G-T
• gnomAD v4: 6-31355066-G-T
• MyVariant Identifiers: chr6:g.31322843G>T (hg19) ; chr6:g.31355066G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355066G>T , CM000668.2:g.31355066G>T	GRCh38
NC_000006.11:g.31322843G>T , CM000668.1:g.31322843G>T	GRCh37
NC_000006.10:g.31430822G>T	NCBI36
NG_023187.1:g.7147C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+41C>A
ENST00000481849.6:n.2619C>A
ENST00000497377.6:n.2526C>A
ENST00000640094.2:c.895+251C>A	ENSP00000491275.2:n.895+251C>A
ENST00000696558.1:c.1081+41C>A	ENSP00000512716.1:n.1081+41C>A
ENST00000696559.1:c.1012+41C>A	ENSP00000512717.1:n.1012+41C>A
ENST00000696560.1:c.1012+41C>A	ENSP00000512718.1:n.1012+41C>A
ENST00000696561.1:c.1012+41C>A	ENSP00000512719.1:n.1012+41C>A
ENST00000696562.1:c.1012+41C>A	ENSP00000512720.1:n.1012+41C>A
ENST00000412585.7:c.1012+41C>A MANE Select	ENSP00000399168.2:n.1012+41C>A
ENST00000640094.1:c.88+251C>A	ENSP00000491275.1:n.88+251C>A
ENST00000412585.6:c.1012+41C>A	ENSP00000399168.2:n.1012+41C>A
ENST00000497377.5:n.11C>A
NM_005514.6:c.1012+41C>A	NP_005505.2:n.1012+41C>A
XM_011514556.1:c.1045+41C>A	XP_011512858.1:n.1045+41C>A
XM_011514557.1:c.895+251C>A	XP_011512859.1:n.895+251C>A
XR_926175.1:n.1451+41C>A
NM_005514.7:c.1012+41C>A	NP_005505.2:n.1012+41C>A
NM_005514.8:c.1012+41C>A MANE Select	NP_005505.2:n.1012+41C>A