Canonical Allele Identifier: CA2664004013
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868781G>T , CM000664.2:g.240868781G>T GRCh38
NC_000002.11:g.241808198G>T , CM000664.1:g.241808198G>T GRCh37
NC_000002.10:g.241456871G>T NCBI36
NG_008005.1:g.5037G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-85G>T ENSP00000302620.3:n.-85G>T
NM_000030.2:c.-85G>T NP_000021.1:n.-85G>T
XR_924060.1:n.405+1452C>A