Canonical Allele Identifier: CA2664008756
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875059C>T , CM000664.2:g.240875059C>T GRCh38
NC_000002.11:g.241814476C>T , CM000664.1:g.241814476C>T GRCh37
NC_000002.10:g.241463149C>T NCBI36
NG_008005.1:g.11315C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.681-50C>T MANE Select ENSP00000302620.3:n.681-50C>T
ENST00000307503.3:c.681-50C>T ENSP00000302620.3:n.681-50C>T
ENST00000476698.1:n.333-50C>T
NM_000030.2:c.681-50C>T NP_000021.1:n.681-50C>T
NM_000030.3:c.681-50C>T MANE Select NP_000021.1:n.681-50C>T