Canonical Allele Identifier: CA3711798
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1065386
gnomAD v2: 6-31324547-G-C
gnomAD v3: 6-31356770-G-C
gnomAD v4: 6-31356770-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356770G>C , CM000668.2:g.31356770G>C GRCh38
NC_000006.11:g.31324547G>C , CM000668.1:g.31324547G>C GRCh37
NC_000006.10:g.31432526G>C NCBI36
NG_023187.1:g.5443C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1734C>G
ENST00000481849.6:n.1734C>G
ENST00000497377.6:n.1734C>G
ENST00000640094.2:c.261C>G ENSP00000491275.2:p.Asn87Lys
ENST00000696558.1:c.261C>G ENSP00000512716.1:p.Asn87Lys
ENST00000696559.1:c.261C>G ENSP00000512717.1:p.Asn87Lys
ENST00000696560.1:c.261C>G ENSP00000512718.1:p.Asn87Lys
ENST00000696561.1:c.261C>G ENSP00000512719.1:p.Asn87Lys
ENST00000696562.1:c.261C>G ENSP00000512720.1:p.Asn87Lys
ENST00000412585.7:c.261C>G MANE Select ENSP00000399168.2:p.Asn87Lys
ENST00000412585.6:c.261C>G ENSP00000399168.2:p.Asn87Lys
ENST00000434333.1:c.294C>G ENSP00000405931.1:p.Asn98Lys
ENST00000474381.1:n.136C>G
ENST00000498007.1:n.282C>G
ENST00000603274.1:n.124G>C
NM_005514.6:c.261C>G NP_005505.2:p.Asn87Lys
XM_011514556.1:c.294C>G XP_011512858.1:p.Asn98Lys
XM_011514557.1:c.261C>G XP_011512859.1:p.Asn87Lys
XR_926175.1:n.271C>G
NM_005514.7:c.261C>G NP_005505.2:p.Asn87Lys
NM_005514.8:c.261C>G MANE Select NP_005505.2:p.Asn87Lys