Canonical Allele Identifier: CA448984976
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233360G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233132G>T , CM000668.2:g.26233132G>T GRCh38
NC_000006.11:g.26233360G>T , CM000668.1:g.26233360G>T GRCh37
NC_000006.10:g.26341339G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.11G>T
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