Canonical Allele Identifier: CA448985303
Gene: H2AC9P HGNC NCBI

Linked Data

dbSNP Id: rs1173911218
gnomAD v3: 6-26233187-G-C
gnomAD v4: 6-26233187-G-C
MyVariant Identifiers: chr6:g.26233415G>C (hg19) chr6:g.26233187G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233187G>C , CM000668.2:g.26233187G>C GRCh38
NC_000006.11:g.26233415G>C , CM000668.1:g.26233415G>C GRCh37
NC_000006.10:g.26341394G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.66G>C
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