Canonical Allele Identifier: CA448984954
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233357A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233129A>C , CM000668.2:g.26233129A>C GRCh38
NC_000006.11:g.26233357A>C , CM000668.1:g.26233357A>C GRCh37
NC_000006.10:g.26341336A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.8A>C
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