Canonical Allele Identifier: CA565966866

Linked Data

dbSNP Id: rs1300801169
gnomAD v2: 6-26107489-A-G
gnomAD v3: 6-26107261-A-G
gnomAD v4: 6-26107261-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107261A>G , CM000668.2:g.26107261A>G GRCh38
NC_000006.11:g.26107489A>G , CM000668.1:g.26107489A>G GRCh37
NC_000006.10:g.26215468A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16227T>C (H2BC4) ENSP00000516775.1:n.391-16227T>C
ENST00000629531.1:c.132+16512T>C (H2BC3) ENSP00000486472.1:n.132+16512T>C