Canonical Allele Identifier: CA363573646
Gene: HLA-DOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32782149G>C (hg19) chr6:g.32814372G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32814372G>C , CM000668.2:g.32814372G>C GRCh38
NC_000006.11:g.32782149G>C , CM000668.1:g.32782149G>C GRCh37
NC_000006.10:g.32890127G>C NCBI36
NG_009793.3:g.29399C>G
NG_012008.1:g.7677C>G
NG_009793.4:g.29399C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000438763.7:c.591C>G MANE Select ENSP00000390020.2:p.Tyr197Ter
ENST00000648009.1:c.591C>G ENSP00000496848.1:p.Tyr197Ter
ENST00000438763.6:c.591C>G ENSP00000390020.2:p.Tyr197Ter
ENST00000447394.1:c.541C>G
ENST00000452392.2:c.2412C>G ENSP00000391806.2:p.Tyr804Ter
ENST00000475235.1:n.628C>G
ENST00000488325.5:c.*362C>G ENSP00000436618.1:n.*362C>G
NM_002120.3:c.591C>G NP_002111.1:p.Tyr197Ter
NM_002120.4:c.591C>G MANE Select NP_002111.1:p.Tyr197Ter
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Search 100 bp 3'