Canonical Allele Identifier: CA449747261
Gene: HLA-DOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32782137G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32814360G>T , CM000668.2:g.32814360G>T GRCh38
NC_000006.11:g.32782137G>T , CM000668.1:g.32782137G>T GRCh37
NC_000006.10:g.32890115G>T NCBI36
NG_009793.3:g.29411C>A
NG_012008.1:g.7689C>A
NG_009793.4:g.29411C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000438763.7:c.603C>A MANE Select ENSP00000390020.2:p.Val201=
ENST00000648009.1:c.603C>A ENSP00000496848.1:p.Val201=
ENST00000438763.6:c.603C>A ENSP00000390020.2:p.Val201=
ENST00000452392.2:c.2424C>A ENSP00000391806.2:p.Val808=
ENST00000475235.1:n.640C>A
ENST00000488325.5:c.*374C>A ENSP00000436618.1:n.*374C>A
NM_002120.3:c.603C>A NP_002111.1:p.Val201=
NM_002120.4:c.603C>A MANE Select NP_002111.1:p.Val201=