Canonical Allele Identifier: CA12228642

Linked Data

dbSNP Id: rs198846
gnomAD v2: 6-26107463-A-G
gnomAD v3: 6-26107235-A-G
gnomAD v4: 6-26107235-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107235A>G , CM000668.2:g.26107235A>G GRCh38
NC_000006.11:g.26107463A>G , CM000668.1:g.26107463A>G GRCh37
NC_000006.10:g.26215442A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16201T>C (H2BC4) ENSP00000516775.1:n.391-16201T>C
ENST00000629531.1:c.132+16538T>C (H2BC3) ENSP00000486472.1:n.132+16538T>C