Canonical Allele Identifier: CA448985562

Gene: H2AC9P

Linked Data

• dbSNP Id: rs1291904566
• MyVariant Identifiers: chr6:g.26233460T>C (hg19) ; chr6:g.26233232T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233232T>C , CM000668.2:g.26233232T>C	GRCh38
NC_000006.11:g.26233460T>C , CM000668.1:g.26233460T>C	GRCh37
NC_000006.10:g.26341439T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.111T>C