Canonical Allele Identifier: CA1339336356
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1374742681
gnomAD v4: 2-240879223-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879223G>T , CM000664.2:g.240879223G>T GRCh38
NC_000002.11:g.241818640G>T , CM000664.1:g.241818640G>T GRCh37
NC_000002.10:g.241467313G>T NCBI36
NG_008005.1:g.15479G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*402G>T MANE Select ENSP00000302620.3:n.*402G>T
ENST00000470255.1:n.1359G>T
NM_000030.3:c.*402G>T MANE Select NP_000021.1:n.*402G>T
Search 100 bp 5'
Search 100 bp 3'