Canonical Allele Identifier: CA136836425
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1050388

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356729C>G , CM000668.2:g.31356729C>G GRCh38
NC_000006.11:g.31324506C>G , CM000668.1:g.31324506C>G GRCh37
NC_000006.10:g.31432485C>G NCBI36
NG_023187.1:g.5484G>C

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.302G>C VV NP_005505.2:p.Ser101Thr
XM_011514556.1:c.335G>C XP_011512858.1:p.Ser112Thr
XM_011514557.1:c.302G>C XP_011512859.1:p.Ser101Thr
XR_926175.1:n.312G>C
NM_005514.7:c.302G>C VV NP_005505.2:p.Ser101Thr
NM_005514.8:c.302G>C VV MANE Preferred NP_005505.2:p.Ser101Thr
ENST00000412585.6:c.302G>C ENSP00000399168.2:p.Ser101Thr
ENST00000434333.1:c.335G>C ENSP00000405931.1:p.Ser112Thr
ENST00000474381.1:n.177G>C
ENST00000498007.1:n.323G>C
ENST00000603274.1:n.83C>G