Canonical Allele Identifier: CA513685578

Gene:

Linked Data

• dbSNP Id: rs2123695033
• gnomAD v4: 22-23573068-A-T
• MyVariant Identifiers: chr22:g.23915255A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573068A>T , CM000684.2:g.23573068A>T	GRCh38
NC_000022.10:g.23915255A>T , CM000684.1:g.23915255A>T	GRCh37
NC_000022.9:g.22245255A>T	NCBI36
NG_009791.1:g.12241T>A , LRG_69:g.12241T>A

Transcript Alleles

HGVS	Amino-acid Change
XR_938075.1:n.709A>T
XR_938076.1:n.774A>T
XR_938078.1:n.673A>T
XR_938079.1:n.566A>T
XR_938075.2:n.1293A>T
XR_938078.2:n.1257A>T