Canonical Allele Identifier: CA2577301962
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868859G>C , CM000664.2:g.240868859G>C GRCh38
NC_000002.11:g.241808276G>C , CM000664.1:g.241808276G>C GRCh37
NC_000002.10:g.241456949G>C NCBI36
NG_008005.1:g.5115G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.-7G>C MANE Select ENSP00000302620.3:n.-7G>C
ENST00000307503.3:c.-7G>C ENSP00000302620.3:n.-7G>C
ENST00000472436.1:n.14G>C
NM_000030.2:c.-7G>C NP_000021.1:n.-7G>C
XR_924060.1:n.405+1374C>G
NM_000030.3:c.-7G>C MANE Select NP_000021.1:n.-7G>C