Canonical Allele Identifier: CA766959781
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1194076223
gnomAD v4: 2-240868832-C-T
MyVariant Identifiers: chr2:g.241808249C>T (hg19) chr2:g.240868832C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868832C>T , CM000664.2:g.240868832C>T GRCh38
NC_000002.11:g.241808249C>T , CM000664.1:g.241808249C>T GRCh37
NC_000002.10:g.241456922C>T NCBI36
NG_008005.1:g.5088C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.-34C>T MANE Select ENSP00000302620.3:n.-34C>T
ENST00000307503.3:c.-34C>T ENSP00000302620.3:n.-34C>T
NM_000030.2:c.-34C>T NP_000021.1:n.-34C>T
XR_924060.1:n.405+1401G>A
NM_000030.3:c.-34C>T MANE Select NP_000021.1:n.-34C>T
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