Canonical Allele Identifier: CA1616896845

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107245C= , CM000668.2:g.26107245C= GRCh38
NC_000006.11:g.26107473C= , CM000668.1:g.26107473C= GRCh37
NC_000006.10:g.26215452C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16211G= (H2BC4) ENSP00000516775.1:n.391-16211G=
ENST00000629531.1:c.132+16528G= (H2BC3) ENSP00000486472.1:n.132+16528G=