Canonical Allele Identifier: CA1087073517

Linked Data

dbSNP Id: rs1763262830
gnomAD v3: 6-26107194-C-T
gnomAD v4: 6-26107194-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107194C>T , CM000668.2:g.26107194C>T GRCh38
NC_000006.11:g.26107422C>T , CM000668.1:g.26107422C>T GRCh37
NC_000006.10:g.26215401C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16160G>A (H2BC4) ENSP00000516775.1:n.391-16160G>A
ENST00000629531.1:c.132+16579G>A (H2BC3) ENSP00000486472.1:n.132+16579G>A