Canonical Allele Identifier: CA2664012148
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878564-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878564G>C , CM000664.2:g.240878564G>C GRCh38
NC_000002.11:g.241817981G>C , CM000664.1:g.241817981G>C GRCh37
NC_000002.10:g.241466654G>C NCBI36
NG_008005.1:g.14820G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1072-150G>C MANE Select ENSP00000302620.3:n.1072-150G>C
ENST00000307503.3:c.1072-150G>C ENSP00000302620.3:n.1072-150G>C
ENST00000470255.1:n.850-150G>C
NM_000030.2:c.1072-150G>C NP_000021.1:n.1072-150G>C
NM_000030.3:c.1072-150G>C MANE Select NP_000021.1:n.1072-150G>C
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