Canonical Allele Identifier: CA565966808
Gene: H2BC4 HGNC NCBI
H2BC3 HGNC NCBI

Linked Data

dbSNP Id: rs1474864609
gnomAD v2: 6-26107316-G-A
gnomAD v3: 6-26107088-G-A
gnomAD v4: 6-26107088-G-A
MyVariant Identifiers: chr6:g.26107316G>A (hg19) chr6:g.26107088G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107088G>A , CM000668.2:g.26107088G>A GRCh38
NC_000006.11:g.26107316G>A , CM000668.1:g.26107316G>A GRCh37
NC_000006.10:g.26215295G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16054C>T (H2BC4) ENSP00000516775.1:n.391-16054C>T
ENST00000629531.1:c.132+16685C>T (H2BC3) ENSP00000486472.1:n.132+16685C>T
Search 100 bp 5'
Search 100 bp 3'