Canonical Allele Identifier: CA2677608436

Linked Data

gnomAD v4: 6-26107272-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107272G>A , CM000668.2:g.26107272G>A GRCh38
NC_000006.11:g.26107500G>A , CM000668.1:g.26107500G>A GRCh37
NC_000006.10:g.26215479G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16238C>T (H2BC4) ENSP00000516775.1:n.391-16238C>T
ENST00000629531.1:c.132+16501C>T (H2BC3) ENSP00000486472.1:n.132+16501C>T