Canonical Allele Identifier: CA136260218
Gene: H2BC4 HGNC NCBI
H2BC3 HGNC NCBI

Linked Data

dbSNP Id: rs182849984
gnomAD v3: 6-26107067-G-C
gnomAD v4: 6-26107067-G-C
MyVariant Identifiers: chr6:g.26107295G>C (hg19) chr6:g.26107067G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107067G>C , CM000668.2:g.26107067G>C GRCh38
NC_000006.11:g.26107295G>C , CM000668.1:g.26107295G>C GRCh37
NC_000006.10:g.26215274G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16033C>G (H2BC4) ENSP00000516775.1:n.391-16033C>G
ENST00000629531.1:c.132+16706C>G (H2BC3) ENSP00000486472.1:n.132+16706C>G
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