Canonical Allele Identifier: CA2664004919
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869068C>T , CM000664.2:g.240869068C>T GRCh38
NC_000002.11:g.241808485C>T , CM000664.1:g.241808485C>T GRCh37
NC_000002.10:g.241457158C>T NCBI36
NG_008005.1:g.5324C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+38C>T MANE Select ENSP00000302620.3:n.165+38C>T
ENST00000307503.3:c.165+38C>T ENSP00000302620.3:n.165+38C>T
ENST00000472436.1:n.185+38C>T
NM_000030.2:c.165+38C>T NP_000021.1:n.165+38C>T
XR_924060.1:n.405+1165G>A
NM_000030.3:c.165+38C>T MANE Select NP_000021.1:n.165+38C>T