Canonical Allele Identifier: CA432027160
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241818199G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878782G>T , CM000664.2:g.240878782G>T GRCh38
NC_000002.11:g.241818199G>T , CM000664.1:g.241818199G>T GRCh37
NC_000002.10:g.241466872G>T NCBI36
NG_008005.1:g.15038G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1140G>T MANE Select ENSP00000302620.3:p.Leu380=
ENST00000307503.3:c.1140G>T ENSP00000302620.3:p.Leu380=
ENST00000470255.1:n.918G>T
NM_000030.2:c.1140G>T NP_000021.1:p.Leu380=
NM_000030.3:c.1140G>T MANE Select NP_000021.1:p.Leu380=