Canonical Allele Identifier: CA2770369826

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107086C>G , CM000668.2:g.26107086C>G GRCh38
NC_000006.11:g.26107314C>G , CM000668.1:g.26107314C>G GRCh37
NC_000006.10:g.26215293C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16052G>C (H2BC4) ENSP00000516775.1:n.391-16052G>C
ENST00000629531.1:c.132+16687G>C (H2BC3) ENSP00000486472.1:n.132+16687G>C