Canonical Allele Identifier: CA2664012059
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878217-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878217G>T , CM000664.2:g.240878217G>T GRCh38
NC_000002.11:g.241817634G>T , CM000664.1:g.241817634G>T GRCh37
NC_000002.10:g.241466307G>T NCBI36
NG_008005.1:g.14473G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1071+67G>T MANE Select ENSP00000302620.3:n.1071+67G>T
ENST00000307503.3:c.1071+67G>T ENSP00000302620.3:n.1071+67G>T
ENST00000470255.1:n.849+67G>T
NM_000030.2:c.1071+67G>T NP_000021.1:n.1071+67G>T
NM_000030.3:c.1071+67G>T MANE Select NP_000021.1:n.1071+67G>T
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