Canonical Allele Identifier: CA2677608434

Linked Data

gnomAD v4: 6-26107269-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107269T>A , CM000668.2:g.26107269T>A GRCh38
NC_000006.11:g.26107497T>A , CM000668.1:g.26107497T>A GRCh37
NC_000006.10:g.26215476T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16235A>T (H2BC4) ENSP00000516775.1:n.391-16235A>T
ENST00000629531.1:c.132+16504A>T (H2BC3) ENSP00000486472.1:n.132+16504A>T