Canonical Allele Identifier: CA1616896723

Linked Data

dbSNP Id: rs1763257164

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107097T>G , CM000668.2:g.26107097T>G GRCh38
NC_000006.11:g.26107325T>G , CM000668.1:g.26107325T>G GRCh37
NC_000006.10:g.26215304T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16063A>C (H2BC4) ENSP00000516775.1:n.391-16063A>C
ENST00000629531.1:c.132+16676A>C (H2BC3) ENSP00000486472.1:n.132+16676A>C