Canonical Allele Identifier: CA351313325
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869028C>T , CM000664.2:g.240869028C>T GRCh38
NC_000002.11:g.241808445C>T , CM000664.1:g.241808445C>T GRCh37
NC_000002.10:g.241457118C>T NCBI36
NG_008005.1:g.5284C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.163C>T MANE Select ENSP00000302620.3:p.Gln55Ter
ENST00000307503.3:c.163C>T ENSP00000302620.3:p.Gln55Ter
ENST00000472436.1:n.183C>T
NM_000030.2:c.163C>T NP_000021.1:p.Gln55Ter
XR_924060.1:n.405+1205G>A
NM_000030.3:c.163C>T MANE Select NP_000021.1:p.Gln55Ter