Canonical Allele Identifier: CA650753052

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107171C>T , CM000668.2:g.26107171C>T GRCh38
NC_000006.11:g.26107399C>T , CM000668.1:g.26107399C>T GRCh37
NC_000006.10:g.26215378C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16137G>A (H2BC4) ENSP00000516775.1:n.391-16137G>A
ENST00000629531.1:c.132+16602G>A (H2BC3) ENSP00000486472.1:n.132+16602G>A