Canonical Allele Identifier: CA1616896722

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107097T= , CM000668.2:g.26107097T= GRCh38
NC_000006.11:g.26107325T= , CM000668.1:g.26107325T= GRCh37
NC_000006.10:g.26215304T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16063A= (H2BC4) ENSP00000516775.1:n.391-16063A=
ENST00000629531.1:c.132+16676A= (H2BC3) ENSP00000486472.1:n.132+16676A=