Canonical Allele Identifier: CA351319458
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878021G>C , CM000664.2:g.240878021G>C GRCh38
NC_000002.11:g.241817438G>C , CM000664.1:g.241817438G>C GRCh37
NC_000002.10:g.241466111G>C NCBI36
NG_008005.1:g.14277G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-1G>C MANE Select ENSP00000302620.3:n.943-1G>C
ENST00000307503.3:c.943-1G>C ENSP00000302620.3:n.943-1G>C
ENST00000470255.1:n.721-1G>C
NM_000030.2:c.943-1G>C NP_000021.1:n.943-1G>C
NM_000030.3:c.943-1G>C MANE Select NP_000021.1:n.943-1G>C