Canonical Allele Identifier: CA12805588
Gene: FAM167A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2002030
gnomAD v2: 8-11276542-T-C
gnomAD v3: 8-11419033-T-C
gnomAD v4: 8-11419033-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11419033T>C , CM000670.2:g.11419033T>C GRCh38
NC_000008.10:g.11276542T>C , CM000670.1:g.11276542T>C GRCh37
NC_000008.9:g.11313952T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_026814.1:n.341-14887T>C