Canonical Allele Identifier: CA68173275

Gene: AGXT

Linked Data

• dbSNP Id: rs768779757
• MyVariant Identifiers: chr2:g.241807985_241807987del (hg19) ; chr2:g.240868568_240868570del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240868569_240868571del , CM000664.2:g.240868569_240868571del	GRCh38
NC_000002.11:g.241807986_241807988del , CM000664.1:g.241807986_241807988del	GRCh37
NC_000002.10:g.241456659_241456661del	NCBI36
NG_008005.1:g.4825_4827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.3:c.-297_-295del	ENSP00000302620.3:n.-297_-295del
XR_924060.1:n.405+1663_405+1665del