Canonical Allele Identifier: CA448985196
Gene: H2AC9P HGNC NCBI

Linked Data

dbSNP Id: rs1033907191
gnomAD v4: 6-26233169-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233169G>T , CM000668.2:g.26233169G>T GRCh38
NC_000006.11:g.26233397G>T , CM000668.1:g.26233397G>T GRCh37
NC_000006.10:g.26341376G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.48G>T