Canonical Allele Identifier: CA1616896788

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107179C= , CM000668.2:g.26107179C= GRCh38
NC_000006.11:g.26107407C= , CM000668.1:g.26107407C= GRCh37
NC_000006.10:g.26215386C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16145G= (H2BC4) ENSP00000516775.1:n.391-16145G=
ENST00000629531.1:c.132+16594G= (H2BC3) ENSP00000486472.1:n.132+16594G=