Canonical Allele Identifier: CA1616944558
Gene: H2BC7 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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