Canonical Allele Identifier: CA351313250
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1279674854

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869007T>C , CM000664.2:g.240869007T>C GRCh38
NC_000002.11:g.241808424T>C , CM000664.1:g.241808424T>C GRCh37
NC_000002.10:g.241457097T>C NCBI36
NG_008005.1:g.5263T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.142T>C MANE Select ENSP00000302620.3:p.Ser48Pro
ENST00000307503.3:c.142T>C ENSP00000302620.3:p.Ser48Pro
ENST00000472436.1:n.162T>C
NM_000030.2:c.142T>C NP_000021.1:p.Ser48Pro
XR_924060.1:n.405+1226A>G
NM_000030.3:c.142T>C MANE Select NP_000021.1:p.Ser48Pro