Canonical Allele Identifier: CA1616896848

Linked Data

dbSNP Id: rs1763264809

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107253_26107254dup , CM000668.2:g.26107253_26107254dup GRCh38
NC_000006.11:g.26107481_26107482dup , CM000668.1:g.26107481_26107482dup GRCh37
NC_000006.10:g.26215460_26215461dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16218_391-16217dup (H2BC4) ENSP00000516775.1:n.391-16218_391-16217dup
ENST00000629531.1:c.132+16521_132+16522dup (H2BC3) ENSP00000486472.1:n.132+16521_132+16522dup