Canonical Allele Identifier: CA1616896710

Linked Data

dbSNP Id: rs1763256859

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107085A>G , CM000668.2:g.26107085A>G GRCh38
NC_000006.11:g.26107313A>G , CM000668.1:g.26107313A>G GRCh37
NC_000006.10:g.26215292A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16051T>C (H2BC4) ENSP00000516775.1:n.391-16051T>C
ENST00000629531.1:c.132+16688T>C (H2BC3) ENSP00000486472.1:n.132+16688T>C