Canonical Allele Identifier: CA351318300
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875941T>G , CM000664.2:g.240875941T>G GRCh38
NC_000002.11:g.241815358T>G , CM000664.1:g.241815358T>G GRCh37
NC_000002.10:g.241464031T>G NCBI36
NG_008005.1:g.12197T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.783T>G MANE Select ENSP00000302620.3:p.His261Gln
ENST00000307503.3:c.783T>G ENSP00000302620.3:p.His261Gln
ENST00000476698.1:n.435T>G
NM_000030.2:c.783T>G NP_000021.1:p.His261Gln
NM_000030.3:c.783T>G MANE Select NP_000021.1:p.His261Gln