Canonical Allele Identifier: CA513685575

Gene:

Linked Data

• gnomAD v4: 22-23573067-G-T
• MyVariant Identifiers: chr22:g.23915254G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573067G>T , CM000684.2:g.23573067G>T	GRCh38
NC_000022.10:g.23915254G>T , CM000684.1:g.23915254G>T	GRCh37
NC_000022.9:g.22245254G>T	NCBI36
NG_009791.1:g.12242C>A , LRG_69:g.12242C>A

Transcript Alleles

HGVS	Amino-acid Change
XR_938075.1:n.708G>T
XR_938076.1:n.773G>T
XR_938078.1:n.672G>T
XR_938079.1:n.565G>T
XR_938075.2:n.1292G>T
XR_938078.2:n.1256G>T