Canonical Allele Identifier: CA2664011641
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240877975-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877975C>T , CM000664.2:g.240877975C>T GRCh38
NC_000002.11:g.241817392C>T , CM000664.1:g.241817392C>T GRCh37
NC_000002.10:g.241466065C>T NCBI36
NG_008005.1:g.14231C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-47C>T MANE Select ENSP00000302620.3:n.943-47C>T
ENST00000307503.3:c.943-47C>T ENSP00000302620.3:n.943-47C>T
ENST00000470255.1:n.721-47C>T
NM_000030.2:c.943-47C>T NP_000021.1:n.943-47C>T
NM_000030.3:c.943-47C>T MANE Select NP_000021.1:n.943-47C>T
Search 100 bp 5'
Search 100 bp 3'