Canonical Allele Identifier: CA2841727856

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107232G>T , CM000668.2:g.26107232G>T GRCh38
NC_000006.11:g.26107460G>T , CM000668.1:g.26107460G>T GRCh37
NC_000006.10:g.26215439G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16198C>A (H2BC4) ENSP00000516775.1:n.391-16198C>A
ENST00000629531.1:c.132+16541C>A (H2BC3) ENSP00000486472.1:n.132+16541C>A