Canonical Allele Identifier: CA1339330705
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868827G= , CM000664.2:g.240868827G= GRCh38
NC_000002.11:g.241808244G= , CM000664.1:g.241808244G= GRCh37
NC_000002.10:g.241456917G= NCBI36
NG_008005.1:g.5083G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.-39G= MANE Select ENSP00000302620.3:n.-39G=
ENST00000307503.3:c.-39G= ENSP00000302620.3:n.-39G=
NM_000030.2:c.-39G= NP_000021.1:n.-39G=
XR_924060.1:n.405+1406C=
NM_000030.3:c.-39G= MANE Select NP_000021.1:n.-39G=