Canonical Allele Identifier: CA12184963
Gene: H2AC9P HGNC NCBI

Linked Data

dbSNP Id: rs10946808
gnomAD v2: 6-26233387-A-G
gnomAD v3: 6-26233159-A-G
gnomAD v4: 6-26233159-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233159A>G , CM000668.2:g.26233159A>G GRCh38
NC_000006.11:g.26233387A>G , CM000668.1:g.26233387A>G GRCh37
NC_000006.10:g.26341366A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.38A>G