Canonical Allele Identifier: CA1087073461

Linked Data

dbSNP Id: rs1763256505
gnomAD v3: 6-26107068-C-A
gnomAD v4: 6-26107068-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107068C>A , CM000668.2:g.26107068C>A GRCh38
NC_000006.11:g.26107296C>A , CM000668.1:g.26107296C>A GRCh37
NC_000006.10:g.26215275C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16034G>T (H2BC4) ENSP00000516775.1:n.391-16034G>T
ENST00000629531.1:c.132+16705G>T (H2BC3) ENSP00000486472.1:n.132+16705G>T