Canonical Allele Identifier: CA766959701

Gene: AGXT

Linked Data

• dbSNP Id: rs1242690470
• gnomAD v4: 2-240868709-CA-C
• MyVariant Identifiers: chr2:g.241808127del (hg19) ; chr2:g.240868710del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240868710del , CM000664.2:g.240868710del	GRCh38
NC_000002.11:g.241808127del , CM000664.1:g.241808127del	GRCh37
NC_000002.10:g.241456800del	NCBI36
NG_008005.1:g.4966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.3:c.-156del	ENSP00000302620.3:n.-156del
XR_924060.1:n.405+1523del