Canonical Allele Identifier: CA766959627

Gene: AGXT

Linked Data

• dbSNP Id: rs1279601043
• gnomAD v4: 2-240868509-A-G
• MyVariant Identifiers: chr2:g.241807926A>G (hg19) ; chr2:g.240868509A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240868509A>G , CM000664.2:g.240868509A>G	GRCh38
NC_000002.11:g.241807926A>G , CM000664.1:g.241807926A>G	GRCh37
NC_000002.10:g.241456599A>G	NCBI36
NG_008005.1:g.4765A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.3:c.-357A>G	ENSP00000302620.3:n.-357A>G
XR_924060.1:n.405+1724T>C