Canonical Allele Identifier: CA432026917
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241818134C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878717C>T , CM000664.2:g.240878717C>T GRCh38
NC_000002.11:g.241818134C>T , CM000664.1:g.241818134C>T GRCh37
NC_000002.10:g.241466807C>T NCBI36
NG_008005.1:g.14973C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1075C>T MANE Select ENSP00000302620.3:p.Leu359=
ENST00000307503.3:c.1075C>T ENSP00000302620.3:p.Leu359=
ENST00000470255.1:n.853C>T
NM_000030.2:c.1075C>T NP_000021.1:p.Leu359=
NM_000030.3:c.1075C>T MANE Select NP_000021.1:p.Leu359=