Canonical Allele Identifier: CA513685587

Gene:

Linked Data

• MyVariant Identifiers: chr22:g.23915258C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573071C>T , CM000684.2:g.23573071C>T	GRCh38
NC_000022.10:g.23915258C>T , CM000684.1:g.23915258C>T	GRCh37
NC_000022.9:g.22245258C>T	NCBI36
NG_009791.1:g.12238G>A , LRG_69:g.12238G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_938075.1:n.712C>T
XR_938076.1:n.777C>T
XR_938078.1:n.676C>T
XR_938079.1:n.569C>T
XR_938075.2:n.1296C>T
XR_938078.2:n.1260C>T