Canonical Allele Identifier: CA766959675

Gene: AGXT

Linked Data

• dbSNP Id: rs1274738057
• gnomAD v3: 2-240868664-AG-A
• gnomAD v4: 2-240868664-AG-A
• MyVariant Identifiers: chr2:g.241808082del (hg19) ; chr2:g.240868665del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240868667del , CM000664.2:g.240868667del	GRCh38
NC_000002.11:g.241808084del , CM000664.1:g.241808084del	GRCh37
NC_000002.10:g.241456757del	NCBI36
NG_008005.1:g.4923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.3:c.-199del	ENSP00000302620.3:n.-199del
XR_924060.1:n.405+1568del