Canonical Allele Identifier: CA1087073468

Linked Data

dbSNP Id: rs1763256784
gnomAD v3: 6-26107077-T-C
gnomAD v4: 6-26107077-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107077T>C , CM000668.2:g.26107077T>C GRCh38
NC_000006.11:g.26107305T>C , CM000668.1:g.26107305T>C GRCh37
NC_000006.10:g.26215284T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16043A>G (H2BC4) ENSP00000516775.1:n.391-16043A>G
ENST00000629531.1:c.132+16696A>G (H2BC3) ENSP00000486472.1:n.132+16696A>G