Canonical Allele Identifier: CA14921896
Gene: FAM230I HGNC NCBI

Linked Data

dbSNP Id: rs6519442

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23471071T>G , CM000684.2:g.23471071T>G GRCh38
NC_000022.10:g.23813258T>G , CM000684.1:g.23813258T>G GRCh37
NC_000022.9:g.22143258T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110539.1:n.465A>C
NR_110539.2:n.465A>C
NR_165488.1:n.434A>C
NR_165489.1:n.465A>C
NR_165490.1:n.465A>C