Canonical Allele Identifier: CA766959736

Gene: AGXT

Linked Data

• dbSNP Id: rs1326776002
• MyVariant Identifiers: chr2:g.241808185del (hg19) ; chr2:g.240868768del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240868768del , CM000664.2:g.240868768del	GRCh38
NC_000002.11:g.241808185del , CM000664.1:g.241808185del	GRCh37
NC_000002.10:g.241456858del	NCBI36
NG_008005.1:g.5024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.3:c.-98del	ENSP00000302620.3:n.-98del
NM_000030.2:c.-98del	NP_000021.1:n.-98del
XR_924060.1:n.405+1465del