Canonical Allele Identifier: CA766962238
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1197768495
gnomAD v4: 2-240871316-G-T
MyVariant Identifiers: chr2:g.241810733G>T (hg19) chr2:g.240871316G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871316G>T , CM000664.2:g.240871316G>T GRCh38
NC_000002.11:g.241810733G>T , CM000664.1:g.241810733G>T GRCh37
NC_000002.10:g.241459406G>T NCBI36
NG_008005.1:g.7572G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.424-33G>T MANE Select ENSP00000302620.3:n.424-33G>T
ENST00000307503.3:c.424-33G>T ENSP00000302620.3:n.424-33G>T
ENST00000472436.1:n.444-33G>T
ENST00000476698.1:n.128G>T
NM_000030.2:c.424-33G>T NP_000021.1:n.424-33G>T
NM_000030.3:c.424-33G>T MANE Select NP_000021.1:n.424-33G>T
Search 100 bp 5'
Search 100 bp 3'