Canonical Allele Identifier: CA2839882526
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873941G>T , CM000664.2:g.240873941G>T GRCh38
NC_000002.11:g.241813358G>T , CM000664.1:g.241813358G>T GRCh37
NC_000002.10:g.241462031G>T NCBI36
NG_008005.1:g.10197G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.596-37G>T MANE Select ENSP00000302620.3:n.596-37G>T
ENST00000307503.3:c.596-37G>T ENSP00000302620.3:n.596-37G>T
ENST00000476698.1:n.332+892G>T
NM_000030.2:c.596-37G>T NP_000021.1:n.596-37G>T
NM_000030.3:c.596-37G>T MANE Select NP_000021.1:n.596-37G>T