Canonical Allele Identifier: CA136833758
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341317
gnomAD v4: 6-31356225-C-G
MyVariant Identifiers: chr6:g.31324002C>G (hg19) chr6:g.31356225C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356225C>G , CM000668.2:g.31356225C>G GRCh38
NC_000006.11:g.31324002C>G , CM000668.1:g.31324002C>G GRCh37
NC_000006.10:g.31431981C>G NCBI36
NG_023187.1:g.5988G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2034G>C
ENST00000481849.6:n.2034G>C
ENST00000497377.6:n.2034G>C
ENST00000640094.2:c.561G>C ENSP00000491275.2:p.Glu187Asp
ENST00000696558.1:c.561G>C ENSP00000512716.1:p.Glu187Asp
ENST00000696559.1:c.561G>C ENSP00000512717.1:p.Glu187Asp
ENST00000696560.1:c.561G>C ENSP00000512718.1:p.Glu187Asp
ENST00000696561.1:c.561G>C ENSP00000512719.1:p.Glu187Asp
ENST00000696562.1:c.561G>C ENSP00000512720.1:p.Glu187Asp
ENST00000412585.7:c.561G>C MANE Select ENSP00000399168.2:p.Glu187Asp
ENST00000412585.6:c.561G>C ENSP00000399168.2:p.Glu187Asp
ENST00000434333.1:c.594G>C ENSP00000405931.1:p.Glu198Asp
ENST00000474381.1:n.436G>C
ENST00000498007.1:n.827G>C
NM_005514.6:c.561G>C NP_005505.2:p.Glu187Asp
XM_011514556.1:c.594G>C XP_011512858.1:p.Glu198Asp
XM_011514557.1:c.561G>C XP_011512859.1:p.Glu187Asp
XR_926175.1:n.571G>C
NM_005514.7:c.561G>C NP_005505.2:p.Glu187Asp
NM_005514.8:c.561G>C MANE Select NP_005505.2:p.Glu187Asp
Search 100 bp 5'
Search 100 bp 3'