Canonical Allele Identifier: CA1616944556
Gene: H2BC7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26200449A= , CM000668.2:g.26200449A= GRCh38
NC_000006.11:g.26200677A= , CM000668.1:g.26200677A= GRCh37
NC_000006.10:g.26308656A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356530.5:c.*510A= ENSP00000348924.3:n.*510A=