Canonical Allele Identifier: CA766959723

Gene: AGXT

Linked Data

• dbSNP Id: rs1467606519
• gnomAD v3: 2-240868742-C-T
• gnomAD v4: 2-240868742-C-T
• MyVariant Identifiers: chr2:g.241808159C>T (hg19) ; chr2:g.240868742C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240868742C>T , CM000664.2:g.240868742C>T	GRCh38
NC_000002.11:g.241808159C>T , CM000664.1:g.241808159C>T	GRCh37
NC_000002.10:g.241456832C>T	NCBI36
NG_008005.1:g.4998C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.3:c.-124C>T	ENSP00000302620.3:n.-124C>T
XR_924060.1:n.405+1491G>A