Canonical Allele Identifier: CA136260223
Gene: H2BC4 HGNC NCBI
H2BC3 HGNC NCBI

Linked Data

dbSNP Id: rs554808410
gnomAD v3: 6-26107070-T-G
gnomAD v4: 6-26107070-T-G
MyVariant Identifiers: chr6:g.26107298T>G (hg19) chr6:g.26107070T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107070T>G , CM000668.2:g.26107070T>G GRCh38
NC_000006.11:g.26107298T>G , CM000668.1:g.26107298T>G GRCh37
NC_000006.10:g.26215277T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16036A>C (H2BC4) ENSP00000516775.1:n.391-16036A>C
ENST00000629531.1:c.132+16703A>C (H2BC3) ENSP00000486472.1:n.132+16703A>C
Search 100 bp 5'
Search 100 bp 3'