Canonical Allele Identifier: CA432023208
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241810831G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871414G>C , CM000664.2:g.240871414G>C GRCh38
NC_000002.11:g.241810831G>C , CM000664.1:g.241810831G>C GRCh37
NC_000002.10:g.241459504G>C NCBI36
NG_008005.1:g.7670G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.489G>C MANE Select ENSP00000302620.3:p.Leu163=
ENST00000307503.3:c.489G>C ENSP00000302620.3:p.Leu163=
ENST00000472436.1:n.509G>C
ENST00000476698.1:n.226G>C
NM_000030.2:c.489G>C NP_000021.1:p.Leu163=
NM_000030.3:c.489G>C MANE Select NP_000021.1:p.Leu163=