Canonical Allele Identifier: CA420653787
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs782807933
MyVariant Identifiers: chr1:g.149856162_149856171del (hg19) chr1:g.149884612_149884621del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884615_149884624del , CM000663.2:g.149884615_149884624del GRCh38
NC_000001.10:g.149856165_149856174del , CM000663.1:g.149856165_149856174del GRCh37
NC_000001.9:g.148122789_148122798del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1639_*1648del MANE Select ENSP00000358151.2:n.*1639_*1648del
ENST00000369155.3:c.*1639_*1648del ENSP00000358151.2:n.*1639_*1648del
ENST00000369160.3:c.377+1643_377+1652del ENSP00000375736.2:n.377+1643_377+1652del
NM_003528.2:c.*1639_*1648del NP_003519.1:n.*1639_*1648del
NM_003528.3:c.*1639_*1648del MANE Select NP_003519.1:n.*1639_*1648del
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