Canonical Allele Identifier: CA136260423

Linked Data

dbSNP Id: rs917365320
gnomAD v2: 6-26107475-C-G
gnomAD v3: 6-26107247-C-G
gnomAD v4: 6-26107247-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107247C>G , CM000668.2:g.26107247C>G GRCh38
NC_000006.11:g.26107475C>G , CM000668.1:g.26107475C>G GRCh37
NC_000006.10:g.26215454C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16213G>C (H2BC4) ENSP00000516775.1:n.391-16213G>C
ENST00000629531.1:c.132+16526G>C (H2BC3) ENSP00000486472.1:n.132+16526G>C