Canonical Allele Identifier: CA1616896717

Linked Data

dbSNP Id: rs1763257022

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107089T>C , CM000668.2:g.26107089T>C GRCh38
NC_000006.11:g.26107317T>C , CM000668.1:g.26107317T>C GRCh37
NC_000006.10:g.26215296T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16055A>G (H2BC4) ENSP00000516775.1:n.391-16055A>G
ENST00000629531.1:c.132+16684A>G (H2BC3) ENSP00000486472.1:n.132+16684A>G