Canonical Allele Identifier: CA1616896704

Linked Data

dbSNP Id: rs1763256646

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107072T>G , CM000668.2:g.26107072T>G GRCh38
NC_000006.11:g.26107300T>G , CM000668.1:g.26107300T>G GRCh37
NC_000006.10:g.26215279T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16038A>C (H2BC4) ENSP00000516775.1:n.391-16038A>C
ENST00000629531.1:c.132+16701A>C (H2BC3) ENSP00000486472.1:n.132+16701A>C