Canonical Allele Identifier: CA136260228
Gene: H2BC4 HGNC NCBI
H2BC3 HGNC NCBI

Linked Data

dbSNP Id: rs1009388328
gnomAD v2: 6-26107299-G-A
gnomAD v3: 6-26107071-G-A
gnomAD v4: 6-26107071-G-A
MyVariant Identifiers: chr6:g.26107299G>A (hg19) chr6:g.26107071G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107071G>A , CM000668.2:g.26107071G>A GRCh38
NC_000006.11:g.26107299G>A , CM000668.1:g.26107299G>A GRCh37
NC_000006.10:g.26215278G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16037C>T (H2BC4) ENSP00000516775.1:n.391-16037C>T
ENST00000629531.1:c.132+16702C>T (H2BC3) ENSP00000486472.1:n.132+16702C>T
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