Canonical Allele Identifier: CA136260358

Gene: H2BC4 H2BC3

Linked Data

• dbSNP Id: rs764398339
• MyVariant Identifiers: chr6:g.26107432A>G (hg19) ; chr6:g.26107204A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26107204A>G , CM000668.2:g.26107204A>G	GRCh38
NC_000006.11:g.26107432A>G , CM000668.1:g.26107432A>G	GRCh37
NC_000006.10:g.26215411A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707188.1:c.391-16170T>C (H2BC4)	ENSP00000516775.1:n.391-16170T>C
ENST00000629531.1:c.132+16569T>C (H2BC3)	ENSP00000486472.1:n.132+16569T>C