Canonical Allele Identifier: CA351319591
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878091T>C , CM000664.2:g.240878091T>C GRCh38
NC_000002.11:g.241817508T>C , CM000664.1:g.241817508T>C GRCh37
NC_000002.10:g.241466181T>C NCBI36
NG_008005.1:g.14347T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1012T>C MANE Select ENSP00000302620.3:p.Tyr338His
ENST00000307503.3:c.1012T>C ENSP00000302620.3:p.Tyr338His
ENST00000470255.1:n.790T>C
NM_000030.2:c.1012T>C NP_000021.1:p.Tyr338His
NM_000030.3:c.1012T>C MANE Select NP_000021.1:p.Tyr338His