Canonical Allele Identifier: CA136260720
Gene: H2AC9P HGNC NCBI

Linked Data

dbSNP Id: rs911537232
gnomAD v2: 6-26233443-G-T
gnomAD v3: 6-26233215-G-T
gnomAD v4: 6-26233215-G-T
MyVariant Identifiers: chr6:g.26233443G>T (hg19) chr6:g.26233215G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233215G>T , CM000668.2:g.26233215G>T GRCh38
NC_000006.11:g.26233443G>T , CM000668.1:g.26233443G>T GRCh37
NC_000006.10:g.26341422G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.94G>T
Search 100 bp 5'
Search 100 bp 3'