Canonical Allele Identifier: CA351313127
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868975T>C , CM000664.2:g.240868975T>C GRCh38
NC_000002.11:g.241808392T>C , CM000664.1:g.241808392T>C GRCh37
NC_000002.10:g.241457065T>C NCBI36
NG_008005.1:g.5231T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.110T>C MANE Select ENSP00000302620.3:p.Ile37Thr
ENST00000307503.3:c.110T>C ENSP00000302620.3:p.Ile37Thr
ENST00000472436.1:n.130T>C
NM_000030.2:c.110T>C NP_000021.1:p.Ile37Thr
XR_924060.1:n.405+1258A>G
NM_000030.3:c.110T>C MANE Select NP_000021.1:p.Ile37Thr