Canonical Allele Identifier: CA2664009476
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240875903-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875903G>A , CM000664.2:g.240875903G>A GRCh38
NC_000002.11:g.241815320G>A , CM000664.1:g.241815320G>A GRCh37
NC_000002.10:g.241463993G>A NCBI36
NG_008005.1:g.12159G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.777-32G>A MANE Select ENSP00000302620.3:n.777-32G>A
ENST00000307503.3:c.777-32G>A ENSP00000302620.3:n.777-32G>A
ENST00000476698.1:n.429-32G>A
NM_000030.2:c.777-32G>A NP_000021.1:n.777-32G>A
NM_000030.3:c.777-32G>A MANE Select NP_000021.1:n.777-32G>A
Search 100 bp 5'
Search 100 bp 3'