Canonical Allele Identifier: CA3711226
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2442717

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354693C>G , CM000668.2:g.31354693C>G GRCh38
NC_000006.11:g.31322470C>G , CM000668.1:g.31322470C>G GRCh37
NC_000006.10:g.31430449C>G NCBI36
NG_023187.1:g.7520G>C

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.1013-28G>C VV NP_005505.2:p.=
XM_011514556.1:c.1046-28G>C XP_011512858.1:p.=
XM_011514557.1:c.896-28G>C XP_011512859.1:p.=
XR_926175.1:n.1452-28G>C
NM_005514.7:c.1013-28G>C VV NP_005505.2:p.=
NM_005514.8:c.1013-28G>C VV MANE Preferred NP_005505.2:p.=
ENST00000412585.6:c.1013-28G>C ENSP00000399168.2:p.=
ENST00000481849.5:n.114G>C
ENST00000497377.5:n.384G>C