Canonical Allele Identifier: CA1616896699

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107067G= , CM000668.2:g.26107067G= GRCh38
NC_000006.11:g.26107295G= , CM000668.1:g.26107295G= GRCh37
NC_000006.10:g.26215274G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16033C= (H2BC4) ENSP00000516775.1:n.391-16033C=
ENST00000629531.1:c.132+16706C= (H2BC3) ENSP00000486472.1:n.132+16706C=