Canonical Allele Identifier: CA2770369828

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107145C>A , CM000668.2:g.26107145C>A GRCh38
NC_000006.11:g.26107373C>A , CM000668.1:g.26107373C>A GRCh37
NC_000006.10:g.26215352C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16111G>T (H2BC4) ENSP00000516775.1:n.391-16111G>T
ENST00000629531.1:c.132+16628G>T (H2BC3) ENSP00000486472.1:n.132+16628G>T