Canonical Allele Identifier: CA823453051

Linked Data

dbSNP Id: rs1168407257
gnomAD v3: 6-26107236-A-T
gnomAD v4: 6-26107236-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107236A>T , CM000668.2:g.26107236A>T GRCh38
NC_000006.11:g.26107464A>T , CM000668.1:g.26107464A>T GRCh37
NC_000006.10:g.26215443A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16202T>A (H2BC4) ENSP00000516775.1:n.391-16202T>A
ENST00000629531.1:c.132+16537T>A (H2BC3) ENSP00000486472.1:n.132+16537T>A